chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6131846227131846228GC51GENIChomozygous118737302
6131881764131881765TC49GENIChomozygous118633774
6131883409131883410GC38GENIChomozygous114990325
6131912264131912265TC45GENIChomozygous118737305
6131913134131913135GA60GENIChomozygous118576003
6131914487131914488GT49GENIChomozygous118737306
6131915396131915397CG22GENIChomozygous118576004
6131916109131916110AT19GENIChomozygous118576006
6131916110131916111TC19GENIChomozygous118576007
6131917648131917649CT40GENIChomozygous118737307
6131917716131917717AG37GENICpossibly homozygous118576013
6131917844131917845GA56GENIChomozygous118737308
6131918402131918403CT57GENIChomozygous118576015
6131918417131918418AT56GENIChomozygous118576016
6131920622131920623TC23GENIChomozygous118576018
6131920748131920749GA10GENIChomozygous118737309
6131921058131921059TC27GENIChomozygous118737310
6131922062131922063TG30GENIChomozygous118576019
6131922166131922167GA32GENIChomozygous118576020
6131922412131922413TC17GENIChomozygous118576021
6131922713131922714TC32GENIChomozygous118576022
6131922907131922908GT25GENIChomozygous118576023
6131923722131923723CA7GENIChomozygous118737312
6131924102131924103GA55GENIChomozygous118576026