chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77506155075061551TC59GENIChomozygous115717540
77506252375062524GA56GENIChomozygous116039491
77506368975063690TC45GENIChomozygous116039493
77506373275063733TC51GENIChomozygous115717543
77506378775063788CT67GENIChomozygous115717544
77506400975064010GT49GENICpossibly homozygous116039495
77506436975064370GA10GENIChomozygous116039497
77506525575065256TC76GENIChomozygous115717546
77506613575066136AT47GENIChomozygous115717549
77506614075066141GA53GENIChomozygous116039499
77506623975066240AC66GENIChomozygous115717550
77506703875067039CT78GENIChomozygous115717552
77506868875068689TC30GENIChomozygous115717554
77506869475068695TC26GENIChomozygous115717555
77507082875070829TC49GENIChomozygous115717557
77507094575070946TC18GENIChomozygous115717558
77507489475074895TA65GENICpossibly homozygous115717560
77507607075076071TC89GENIChomozygous115717561
77507649375076494CT59GENICpossibly homozygous116039501
77507699975077000GA62GENIChomozygous115717562
77507727675077277CT53GENIChomozygous116039503
77507822975078230AT74GENICpossibly homozygous116039505
77507861475078615TC84GENICpossibly homozygous115717563
77507948975079490TG58GENICpossibly homozygous116039507
77507999175079992AT80GENIChomozygous115717564
77508157675081577AG71GENIChomozygous116039509
77508252275082523TC72GENIChomozygous116039511
77508574275085743GT41GENIChomozygous116039513
77508604675086047TC80GENIChomozygous115717566
77508605675086057CT79GENIChomozygous115717567
77508788675087887CT60GENIChomozygous115717568
77509058075090581GA84GENIChomozygous115717571
77509249875092499CT74GENIChomozygous115717573
77509250975092510GA70GENIChomozygous116039515
77509290475092905TC60GENIChomozygous115717574
77509802375098024GC38GENIChomozygous115717575
77509820475098205AG36GENIChomozygous115717576