chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105760678057606781TC13GENIChomozygous116604013
105760751257607513AG11GENIChomozygous116604017
105760788257607883TC5GENIChomozygous116604019
105760800957608010GC5GENIChomozygous116604021
105760847957608480GC5GENIChomozygous116604025
105760851557608516AG6GENIChomozygous116604027
105760926257609263CT4GENIChomozygous116604029
105760943157609432TC4GENIChomozygous116604031
105760993457609935GC6GENIChomozygous116604033
105761040857610409AG2GENIChomozygous117060318
105761083857610839AG8GENIChomozygous116604035
105761103957611040GA4GENIChomozygous116604039
105761154557611546TC4GENIChomozygous116785601
105761244957612450CT3GENIChomozygous116785603
105761349657613497GA5GENIChomozygous116785605