chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112071296112071297CT47GENIChomozygous111675326
3112071341112071342AG39GENIChomozygous111675327
3112071349112071350AC42GENIChomozygous111675328
3112072827112072828CG61GENIChomozygous111675329
3112073929112073930CG49GENIChomozygous111675330
3112074048112074049CT55GENIChomozygous111675331
3112074963112074964GT27GENIChomozygous111675332
3112076249112076250AG58GENIChomozygous111675333
3112076523112076524GA44GENIChomozygous111675334
3112076999112077000GA39GENIChomozygous111675335
3112079503112079503T44GENIChomozygous127918793
3112080486112080486T39GENIChomozygous127918794
3112080487112080487TT39GENIChomozygous127918795
3112080488112080488TGTCATAACCTCTTTGTTAT37GENIChomozygous127918796
3112081627112081628TC53GENIChomozygous111675336
3112082003112082004GT38GENIChomozygous111675337
3112082292112082292TTTTTTTC40GENIChomozygous127918797
3112082946112082947GA39GENICpossibly homozygous111675338