chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145399885145399886AC55GENIChomozygous119412372
4145399897145399898AG54GENIChomozygous119412373
4145399982145399982GT60GENIChomozygous132967649
4145400197145400198TC48GENIChomozygous119412374
4145400236145400237GA44GENIChomozygous119412375
4145401226145401227A56GENICpossibly homozygous132967651
4145401390145401390C57GENIChomozygous132967652
4145401565145401566TC61GENIChomozygous119412376
4145401713145401714CT51GENIChomozygous119587735
4145401832145401833AG50GENIChomozygous119315450
4145402877145402878CT57GENIChomozygous119315453
4145403181145403182G57GENIChomozygous132967653
4145403782145403783GA65GENIChomozygous119412377
4145404127145404128AC57GENICpossibly homozygous119315456
4145404317145404318AG55GENIChomozygous119315457
4145404336145404337CT49GENIChomozygous119412378
4145400777145400781TGTA20GENICpossibly homozygous133132022
4145400789145400793TGTG20GENIChomozygous133132023
4145400794145400795GA20GENIChomozygous133140306
4145400808145400809GA33GENIChomozygous133140307
4145401112145401113AG28GENIChomozygous133140308