chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4105609992105609993AG24GENIChomozygous72046300
4105610045105610046CT30GENIChomozygous72046302
4105610051105610052AG30GENIChomozygous72046304
4105610806105610807CT18GENIChomozygous72046306
4105611408105611409CT30GENIChomozygous72046308
4105612400105612401CA17GENIChomozygous72046310
4105612768105612769GT19GENIChomozygous72046312
4105613517105613518TC30GENIChomozygous72046314
4105614887105614888CT15GENIChomozygous72046316
4105614955105614956CT26GENIChomozygous72046318
4105615259105615260CA16GENIChomozygous72046320
4105615673105615674AG21GENIChomozygous72046322
4105615934105615935TC17GENIChomozygous71094918
4105616015105616016TG17GENIChomozygous71094922
4105616021105616022GA17GENIChomozygous72046324
4105616312105616313AG25GENIChomozygous72046326
4105616549105616550GA14GENIChomozygous72046328
4105618344105618345AG17GENIChomozygous71094941