chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226034028226034029AG46GENIChomozygous108558471
1226038803226038804GA58GENIChomozygous108558472
1226039966226039967TA23GENICpossibly homozygous108558473
1226040020226040021AG43GENIChomozygous108558474
1226040089226040090AG53GENIChomozygous108558475
1226040462226040463CA54GENICpossibly homozygous108558476
1226040599226040600CT47GENICpossibly homozygous108558477
1226041329226041330CT58GENIChomozygous108558478
1226042412226042413CT15GENIChomozygous108558479
1226042634226042635TC20GENIChomozygous108558480
1226042729226042730CG26GENIChomozygous108558481
1226042902226042903GT66GENICpossibly homozygous108558482
1226043575226043576GA58GENIChomozygous108558483
1226044349226044350TC42GENICpossibly homozygous108558484
1226044595226044596TC84GENICheterozygous108558485
1226044715226044716GA56GENIChomozygous108558486
1226045555226045556GA62GENIChomozygous108558487
1226046122226046123TC69GENIChomozygous108558488
1226046248226046249CT43GENIChomozygous108558489
1226046364226046365AG58GENIChomozygous108558490
1226046569226046570GT54GENICpossibly homozygous108558491
1226047281226047282CT40GENIChomozygous108558492
1226047316226047317GA52GENIChomozygous108558493
1226047651226047652CT63GENICpossibly homozygous108558494
1226048639226048640GA65GENIChomozygous108558495
1226049110226049111CT35GENIChomozygous108558496