chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55066709850667099CT28GENIChomozygous113792615
55066874050668741AC21GENIChomozygous113792619
55067232850672329TC19GENICheterozygous119039733
55067264350672644TC29GENIChomozygous113792625
55067287050672871CG25GENIChomozygous114200767
55067694650676947GT23GENIChomozygous114200768
55067851150678512TC31GENIChomozygous113792632
55067918750679188GA22GENIChomozygous113792633
55067965950679660TC25GENIChomozygous113792634
55067992050679921GT24GENIChomozygous113792635
55067994650679947AC27GENIChomozygous113792636
55068004550680046CT33GENIChomozygous113792637
55068035850680359TC35GENIChomozygous113792638
55068102750681028GA25GENIChomozygous113792639
55068270750682708TG19GENIChomozygous113792645
55068324250683243AG17GENIChomozygous113792646
55068338250683383TA33GENIChomozygous113792647
55068362350683624CG22GENIChomozygous113792648
55068365750683658GA18GENIChomozygous113792649
55068397050683971TG7GENICheterozygous119039734
55068444050684441CT26GENIChomozygous113792650
55068467150684672TG16GENIChomozygous113792651
55068467750684678AT16GENIChomozygous113792652
55068469950684700AG25GENIChomozygous113792653
55068486450684865GT17GENIChomozygous113792654
55068525850685259TG39GENIChomozygous113792656
55068531350685314AT29GENIChomozygous113792657
55068614150686142AG34GENIChomozygous113792658
55068677350686774CT42GENICpossibly homozygous113792659
55068781350687814AC26GENIChomozygous113792670
55068862450688625TG25GENIChomozygous113792671
55068871350688714TA21GENIChomozygous113792672
55068895450688955TG22GENIChomozygous113792673
55068988850689889CT15GENICpossibly homozygous113792674
55069049550690496AT25GENIChomozygous113792675
55069051850690519AC26GENIChomozygous113792676
55069052350690524GC23GENIChomozygous113792677
55069082950690830AT17GENIChomozygous113792678
55069098950690990CT6GENIChomozygous113792679
55069100350691004GA5GENIChomozygous113792680
55069100550691006GC5GENIChomozygous113792681
55069144250691443CT9GENIChomozygous113792683