chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150466182150466183CT46GENIChomozygous114056360
5150469725150469726AG23GENIChomozygous114056362
5150470115150470116GA64GENIChomozygous114056364
5150471441150471442CA50GENIChomozygous114056366
5150471740150471741TC5GENIChomozygous114155844
5150471836150471837CA6GENIChomozygous114155845
5150471841150471842CG6GENIChomozygous114155846
5150471843150471844CT6GENIChomozygous114155847
5150473090150473091TC44GENIChomozygous114056368
5150477612150477613TG48GENICheterozygous114651564
5150479959150479960CG28GENICheterozygous114651566
5150486691150486692TG47GENIChomozygous114056372
5150490966150490967TG9GENICheterozygous114651568
5150491861150491862GA28GENIChomozygous114056374
5150492020150492021AG41GENICpossibly homozygous114651570
5150492684150492685AT24GENIChomozygous114056376
5150492862150492863CT34GENIChomozygous114056378
5150492887150492888TG31GENIChomozygous114056380
5150495168150495169GA27GENICpossibly homozygous114056382
5150495425150495426AG33GENIChomozygous114155849
5150495452150495453GA23GENIChomozygous114155850
5150495479150495480GT5GENIChomozygous114155851
5150495596150495597GT2GENIChomozygous114651572
5150495630150495631TA34GENIChomozygous114056384
5150495675150495676AC23GENIChomozygous114056386
5150495705150495706TC8GENIChomozygous114056388
5150505302150505303CG4GENIChomozygous114254775
5150505427150505428CG5GENIChomozygous114056392