chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3160324825160324826TC12GENIChomozygous57763231
3160324864160324865AG16GENICpossibly homozygous57763232
3160327256160327257GC10GENICpossibly homozygous57763233
3160328007160328008TTG2GENICheterozygous58241048
3160328018160328019TTG1GENIChomozygous58399364
3160328820160328821AG20GENICheterozygous57763243
3160332734160332735CT6GENIChomozygous58399365
3160333192160333193CT15GENIChomozygous58399366
3160333373160333374CT11GENIChomozygous58399367
3160334539160334540AC19GENICpossibly homozygous57763247
3160334822160334823TC11GENICpossibly homozygous57763248
3160335082160335083CT19GENICpossibly homozygous58399368
3160335594160335595AG17GENIChomozygous57763250
3160339072160339074AC--2GENIChomozygous58697534
3160340033160340034CT6GENICheterozygous57763254
3160340381160340382CA12GENICpossibly homozygous57763255
3160340878160340879CA29GENICpossibly homozygous58399370
3160341067160341068TC21GENICpossibly homozygous58399372