chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189858716189858717AG39GENICpossibly homozygous110172125
2189859499189859500TC69GENIChomozygous110172127
2189860453189860454TG43GENIChomozygous110172129
2189860932189860933TA16GENIChomozygous110172130
2189863286189863287AC38GENIChomozygous110172132
2189863497189863498AT44GENIChomozygous110172134
2189864653189864654AG52GENICpossibly homozygous110172136
2189864806189864807AC46GENIChomozygous110172138
2189865461189865462CT32GENIChomozygous110172140
2189866969189866970CA45GENIChomozygous110172142
2189868889189868890CT15GENIChomozygous110172144
2189869859189869860GT46GENIChomozygous110172146
2189874150189874151CG47GENIChomozygous110172148
2189875021189875022TC37GENIChomozygous110172150
2189876845189876846CT57GENIChomozygous110172152