chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15779421257794213TG22GENIChomozygous108857565
15779574457795745TC29GENIChomozygous108112217
15779591657795917CT26GENIChomozygous108112218
15779770657797707AG20GENIChomozygous108112221
15779934557799346CT17GENIChomozygous108857566
15779989457799895GA21GENIChomozygous108857567
15780045857800459TC27GENIChomozygous108112224
15780096457800965GA29GENIChomozygous108112225
15780102657801027CT30GENIChomozygous108857568
15780128157801282GA25GENIChomozygous108112227
15780273957802740GC18GENIChomozygous108112231
15780296957802970TC39GENIChomozygous108112232
15780299057802991CT44GENIChomozygous108857569
15780344257803443TA26GENIChomozygous108857570
15780356157803562TA7GENIChomozygous108857571
15780813357808134AG6GENIChomozygous108857572
15780824057808241TA7GENIChomozygous108857573
15780833457808335TC15GENIChomozygous108857574
15780839757808398TC15GENIChomozygous108857575
15780866357808664AG25GENIChomozygous108112242
15780868657808687GA22GENIChomozygous108857576
15780884057808841AG35GENIChomozygous108112243
15780898457808985AG34GENIChomozygous108857577
15780899457808995GA36GENIChomozygous108857578
15781073657810737GA21GENIChomozygous108112248
15781326557813266AT30GENIChomozygous108112249
15781465457814655AC16GENIChomozygous108112252
15781502357815024CA45GENIChomozygous109043054
15781551557815516AC26GENIChomozygous108857579
15781552957815530CT29GENIChomozygous108857580
15781649857816499CG26GENIChomozygous108857581
15781678257816783CT28GENIChomozygous108857582
15781701057817011TA9GENIChomozygous108857583
15781766557817666TC14GENIChomozygous108857584
15781792857817929TC30GENIChomozygous108857585
15781851957818520AG22GENIChomozygous108857586
15781900157819002CT24GENIChomozygous108857587
15781903257819033CA27GENIChomozygous108857588