chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1161407088161407089CG32GENICheterozygous62022466
1161407124161407125TC34GENICheterozygous60918636
1161407576161407579CCC---17GENICheterozygous60918638
1161422793161422794CT22GENICheterozygous62022477
1161429866161429867AC18GENICheterozygous62022479
1161429949161429950CT21GENICheterozygous62022480
1161458520161458521CT14GENICheterozygous60918779
1161466479161466480AT11GENICheterozygous60918822
1161487019161487020AC19GENICheterozygous61547859
1161487063161487064GA25GENICheterozygous61547860
1161487159161487160AG21GENICheterozygous61547861
1161487264161487265GA11GENICheterozygous61547862
1161487299161487300TG8GENICheterozygous60918874
1161487308161487309CT8GENICheterozygous61547863
1161515190161515191GA16GENICheterozygous60918991
1161524504161524505AG23GENICheterozygous60919024
1161542260161542262GG--23GENICheterozygous62022537
1161632091161632092GT18GENICheterozygous62022599
1161632198161632199GA24GENICheterozygous62022600
1161696594161696595TG8GENICheterozygous60919331
1161696614161696615AG6GENICheterozygous60919332
1161728788161728789GA27GENICheterozygous60919427
1161741721161741722TG23GENICheterozygous60919507
1161741875161741876A-19GENICheterozygous60919508