chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124149424141494242GA53GENIChomozygous50206845
124149459741494598GGC14GENIChomozygous50206846
124149527041495271TC55GENIChomozygous50206847
124149531941495320GA54GENIChomozygous50206848
124149533141495332CT61GENIChomozygous50206849
124149586441495865CT35GENIChomozygous50206850
124149627741496278AG41GENIChomozygous50206851
124149677341496774TC49GENIChomozygous50206852
124149745041497451GT45GENIChomozygous50206853
124149793641497949CAGCCCCTCCCCG-------------7GENIChomozygous50206854
124149910041499101TC35GENIChomozygous50206855
124149952041499521TC57GENIChomozygous50206856
124149987841499879AT43GENICpossibly homozygous50206857
124150015941500160TC33GENIChomozygous50206858
124150024641500247CT43GENIChomozygous50206859
124150073341500737AAAC----21GENIChomozygous50206860
124150144041501441AT13GENICheterozygous50206861
124150145741501458TTCATC14GENICpossibly homozygous50206862
124150147241501473TTCATC20GENIChomozygous50206863
124150171241501713TC50GENIChomozygous50206864
124150175641501757AG33GENIChomozygous50206865
124150182041501821CCTTTTTTT7GENICheterozygous50206866
124150198541501986A-43GENIChomozygous50206867
124150208841502089AG31GENIChomozygous50206868
124150280841502809TG45GENIChomozygous50206869
124150329541503302TTTCTTT-------31GENIChomozygous50206870
124150437341504375GC--29GENIChomozygous50206871
124150497341504974TC8GENICheterozygous50206872
124150497641504977TC8GENICheterozygous50206873
124150497941504980TC8GENICheterozygous50206874
124150506441505067GAA---8GENICheterozygous50206875
124150510141505102GA11GENICheterozygous50206876
124150510741505108GA11GENICheterozygous50206877
124150511341505114GA13GENICheterozygous50206878
124150511741505120AGG---13GENICheterozygous50206879
124150511941505120GA15GENICheterozygous50206880
124150544441505445TC51GENIChomozygous50206881
124150593541505936AAGATG24GENIChomozygous50206882
124150610541506106CCAAAAAAA7GENICpossibly homozygous50206883
124150692541506926TC55GENIChomozygous50206884
124150847741508478TTA17GENICpossibly homozygous50206885
124150934041509341TTA35GENIChomozygous50206886
124150996441509968GAAC----16GENICheterozygous50206887
124150996841509972AAAA----11GENIChomozygous50206888
124151012441510125GA23GENICheterozygous50206889
124151030141510302AG26GENICpossibly homozygous50206890
124151108941511090CCAA9GENICheterozygous50206891
124151108941511090CCAAA9GENICheterozygous50206892
124151127341511277AGAC----6GENIChomozygous50206893
124151151341511529GTGTGTGTGTGTGTGT----------------2GENIChomozygous50206894
124151159241511593GA50GENICpossibly homozygous50206895
124151173541511736AG29GENIChomozygous50206896
124151179141511794CCC---10GENICheterozygous50206897
124151225941512260A-1GENIChomozygous50206898
124151305141513052CT36GENIChomozygous50206899
124151359241513593GA33GENIChomozygous50206900
124151367141513674AGG---22GENIChomozygous50206901
124151367241513674GG--22GENIChomozygous50206902
124151368341513685AA--16GENIChomozygous50206903
124151404941514060AAAAAAAAAAA-----------17GENICpossibly homozygous50206904
124151437741514378AAAAAC17GENICheterozygous50206905
124151438641514389ACC---15GENICheterozygous50206906
124151438741514389CC--15GENICheterozygous50206907
124151439941514400AAC16GENICheterozygous50206908
124151440741514410AAC---11GENIChomozygous50206909
124151451341514514GGAA11GENICheterozygous50206910
124151451341514514GGA11GENICheterozygous50206911
124151571041515711A-53GENIChomozygous50206912
124151586341515864CT43GENIChomozygous50206913
124151593441515940ACATAC------22GENIChomozygous50206914
124151637941516380GC32GENIChomozygous50206915
124151655841516559TTTC28GENIChomozygous50206916
124151775441517755TA45GENICpossibly homozygous50206917
124151841041518411TC39GENIChomozygous50206918
124151941941519420AC41GENIChomozygous50206919
124151951241519513AAT14GENIChomozygous50206920
124151951841519519CCAT7GENIChomozygous50206921
124151954941519553ATAT----5GENIChomozygous50206922
124152049341520494CT33GENIChomozygous50206923