chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112087343112087344CG16GENIChomozygous112006423
3112087568112087569GT25GENIChomozygous112139313
3112088525112088526GA24GENIChomozygous112006425
3112088594112088595TC27GENIChomozygous112006427
3112088829112088830CT15GENIChomozygous112006429
3112089308112089309TC21GENIChomozygous112006431
3112089575112089576GA18GENIChomozygous111675341
3112095504112095505GA24GENIChomozygous111675349
3112095565112095566CT22GENIChomozygous112139314
3112095583112095584GA25GENIChomozygous112006433
3112095779112095780TA26GENIChomozygous112006435
3112095818112095819CT28GENIChomozygous112006437
3112095832112095833GA24GENIChomozygous112006439
3112095833112095834CA23GENIChomozygous112006441
3112095882112095883CT21GENIChomozygous112006445
3112095897112095898GC22GENIChomozygous112006447
3112095982112095983CT18GENIChomozygous112139315
3112096015112096016CT16GENIChomozygous112006449
3112096088112096089CA19GENIChomozygous112006451
3112096312112096313CT17GENIChomozygous112006453
3112097171112097172AG20GENIChomozygous112006459
3112098204112098205GA9GENIChomozygous112006461
3112098399112098400AG10GENIChomozygous111675351
3112098453112098454GT20GENIChomozygous111675352
3112100304112100305TG11GENIChomozygous111675353
3112105816112105817CT19GENIChomozygous112006469
3112113728112113729GA20GENIChomozygous112139317
3112115866112115867AG13GENIChomozygous111675363
3112119716112119717CT25GENIChomozygous111675364
3112119919112119920AG10GENIChomozygous112006479