chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226070076226070077TC89GENICheterozygous61103630
1226070180226070181GA155GENICheterozygous61103631
1226070856226070857GA108GENIChomozygous61103632
1226075019226075023TGTG----7GENICheterozygous61103633
1226075021226075023TG--7GENICheterozygous61103634
1226075178226075179CT94GENICpossibly homozygous61103635
1226075774226075775TC139GENICheterozygous61103636
1226075837226075838CT116GENICheterozygous61103637
1226075918226075919TG102GENICheterozygous61103638
1226075930226075931G-81GENICheterozygous61103639
1226076312226076313CT102GENICheterozygous61103640
1226078913226078914CG57GENICheterozygous61103641
1226079755226079773TCTCTCTCTCTCTCTCTC------------------13GENICheterozygous61103642
1226081198226081199AT120GENIChomozygous61103643
1226082906226082907AG76GENIChomozygous61103644
1226083274226083275TC72GENIChomozygous61103645
1226083358226083359T-16GENIChomozygous61103646
1226083620226083621TC69GENIChomozygous61103647
1226083993226083994GA35GENICheterozygous61103648
1226084053226084054GA60GENICpossibly homozygous61103649
1226084958226084959TC102GENIChomozygous61103650
1226085439226085440AG92GENICpossibly homozygous61103651
1226085526226085530CACA----73GENICheterozygous61103652
1226085528226085530CA--73GENICpossibly homozygous61103653
1226085589226085590AACG97GENICheterozygous61103654
1226085634226085635TC75GENICheterozygous61103655
1226085662226085663CT44GENICheterozygous61103656
1226086829226086830TA48GENIChomozygous61103657
1226087132226087133G-27GENIChomozygous61103658
1226087314226087315TC35GENIChomozygous61103659
1226087315226087316TC35GENIChomozygous61103660
1226087729226087730CT45GENIChomozygous61103661
1226088742226088743TC57GENIChomozygous61103662