chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172676747126767472AG15GENIChomozygous147145424
172676749126767492CT16GENIChomozygous147145425
172676764626767647AG47GENIChomozygous140088896
172676777326767774TG43GENIChomozygous147145426
172676865526768656GA50GENIChomozygous147145427
172676880126768802AC58GENIChomozygous140088897
172676896826768969CA56GENICpossibly homozygous147145428
172676945226769453GA56GENIChomozygous147145429
172676974426769745AT64GENIChomozygous147145430
172677054926770550CG67GENIChomozygous147145431
172677061026770611GA57GENIChomozygous147145432
172677145926771460AG50GENIChomozygous140088898
172677248826772489CT57GENIChomozygous147145433
172677273226772733GA56GENIChomozygous147145434
172677300526773006CT60GENIChomozygous147145435
172677302826773029CT63GENIChomozygous147145436
172677340326773404TC56GENIChomozygous140088900
172677340826773409TC58GENIChomozygous147145437
172677427226774273GA64GENICpossibly homozygous147145438
172677446626774467AG57GENIChomozygous147145439
172677449526774496AG62GENIChomozygous140088901
172677597526775976TC73GENIChomozygous140088902
172677758826777589GA70GENIChomozygous140088905
172677770526777706GT53GENIChomozygous140088906
172677958926779590CG70GENIChomozygous140088912
172677967126779672CT56GENIChomozygous140088913
172677972526779726TC55GENIChomozygous140088914
172677324826773252TTTG54GENIChomozygous147139650
172677944026779441A42GENICpossibly homozygous140017239
172678156126781562TC47GENIChomozygous140088919
172678417326784174GT45GENIChomozygous147145440
172678490726784908AG45GENIChomozygous140088926
172678565226785653CT64GENIChomozygous147145441
172678838226788383CT51GENIChomozygous140088933
172678874026788741TA58GENIChomozygous147145442
172678909726789098GA39GENIChomozygous147145443
172678978126789782CG54GENIChomozygous147145444