chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6116438245116438246GT39GENIChomozygous54663394
6116439591116439592GA55GENICpossibly homozygous54663398
6116439817116439818GGA76GENICpossibly homozygous54663401
6116439818116439819A-76GENICheterozygous54844632
6116442107116442108GA62GENICpossibly homozygous54663403
6116442452116442453CG18GENIChomozygous54663405
6116443718116443719TA82GENIChomozygous54663407
6116443799116443800G-29GENIChomozygous54663409
6116444045116444046AATGTGTGTG5GENIChomozygous54663411
6116445200116445201AG57GENICpossibly homozygous54663413
6116446111116446112GC72GENIChomozygous54663415