chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4105609992105609993AG21GENIChomozygous72046300
4105610045105610046CT25GENIChomozygous72046302
4105610051105610052AG26GENIChomozygous72046304
4105610806105610807CT13GENIChomozygous72046306
4105611408105611409CT20GENIChomozygous72046308
4105612400105612401CA28GENIChomozygous72046310
4105612768105612769GT23GENIChomozygous72046312
4105613517105613518TC34GENIChomozygous72046314
4105614887105614888CT27GENIChomozygous72046316
4105614955105614956CT26GENIChomozygous72046318
4105615259105615260CA20GENIChomozygous72046320
4105615673105615674AG33GENIChomozygous72046322
4105615934105615935TC24GENIChomozygous71094918
4105616015105616016TG29GENIChomozygous71094922
4105616021105616022GA30GENIChomozygous72046324
4105616312105616313AG30GENIChomozygous72046326
4105616549105616550GA20GENIChomozygous72046328
4105618344105618345AG27GENIChomozygous71094941