chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4105609992105609993AG68GENIChomozygous72046300
4105610045105610046CT45GENIChomozygous72046302
4105610051105610052AG37GENIChomozygous72046304
4105610806105610807CT47GENIChomozygous72046306
4105611408105611409CT49GENICpossibly homozygous72046308
4105612400105612401CA48GENIChomozygous72046310
4105612768105612769GT35GENICpossibly homozygous72046312
4105613517105613518TC34GENIChomozygous72046314
4105614887105614888CT62GENIChomozygous72046316
4105614955105614956CT54GENIChomozygous72046318
4105615259105615260CA38GENIChomozygous72046320
4105615673105615674AG40GENIChomozygous72046322
4105615934105615935TC42GENIChomozygous71094918
4105616015105616016TG52GENIChomozygous71094922
4105616021105616022GA53GENIChomozygous72046324
4105616312105616313AG48GENIChomozygous72046326
4105616549105616550GA69GENIChomozygous72046328
4105618344105618345AG30GENICpossibly homozygous71094941