chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112069232112069233TC55GENIChomozygous112006407
3112071296112071297CT48GENIChomozygous111675326
3112071341112071342AG51GENIChomozygous111675327
3112071349112071350AC47GENIChomozygous111675328
3112073929112073930CG52GENIChomozygous111675330
3112074048112074049CT49GENIChomozygous111675331
3112074491112074492AT77GENIChomozygous112006409
3112074515112074516GA80GENIChomozygous112006411
3112075672112075673GA52GENIChomozygous112006413
3112076249112076250AG59GENIChomozygous111675333
3112080486112080486T49GENIChomozygous127918794
3112080487112080487TT49GENIChomozygous127918795
3112080488112080488TGTCATAACCTCTTTGTTAT48GENIChomozygous127918796
3112080950112080951GC53GENIChomozygous112006415
3112081376112081377AG50GENIChomozygous112006417
3112081627112081628TC54GENIChomozygous111675336
3112082292112082292TTTTTTTC48GENIChomozygous127918797
3112082854112082860ACACGC41GENIChomozygous130908141
3112082945112082945CA21GENICheterozygous130908142
3112082946112082947GA20GENICpossibly homozygous111675338