chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199992840199992841TC10GENIChomozygous61044838
1199992982199992983AG1GENIChomozygous61044839
1199993355199993356GC10GENIChomozygous61044843
1199994087199994088G-15GENIChomozygous61044844
1199994128199994129A-21GENICpossibly homozygous61044845
1199994899199994900CT14GENICpossibly homozygous61044848
1199995938199995939CT19GENIChomozygous61044849
1199997901199997902TC10GENICpossibly homozygous61044852
1199999309199999310CT4GENIChomozygous61044854
1200000500200000501AG9GENIChomozygous61044855
1200000545200000546TC8GENICheterozygous61044856
1200000546200000547TC8GENICheterozygous61044857
1200001048200001049AG2GENIChomozygous61044858
1200002107200002108AT14GENICpossibly homozygous61044859
1200002177200002178TC23GENICpossibly homozygous61044860
1200002528200002529CA12GENICpossibly homozygous61044861
1200003589200003590T-11GENIChomozygous61044862
1200004527200004528GA15GENIChomozygous61044863
1200006624200006625TC9GENICpossibly homozygous61044864
1200006876200006877CT13GENICpossibly homozygous61044865
1200008107200008108CT27GENICpossibly homozygous61044867
1200008253200008254GA25GENIChomozygous61044868
1200008385200008386CA19GENIChomozygous61044869
1200008663200008664CCT14GENIChomozygous61044870
1200008815200008816T-8GENICheterozygous61044871
1200009080200009081CG15GENICpossibly homozygous61044872
1200009168200009169TTA10GENIChomozygous61044873
1200009352200009353TTGAGA2GENIChomozygous61044876
1200009777200009778GT25GENICheterozygous61044880
1200009778200009779GT25GENICheterozygous61044881
1200014895200014896T-6GENICheterozygous61044885
1200016711200016712TG9GENIChomozygous61044887
1200017254200017256AA--1GENIChomozygous61317221
1200020966200020967GA12GENICpossibly homozygous61044889
1200022798200022799CCG7GENICheterozygous62095517
1200022970200022971TC8GENIChomozygous61044891