chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109021144190211442GA14GENIChomozygous68165194
109021235690212357GA15GENIChomozygous68165197
109021417790214178CT18GENIChomozygous68455203
109021430390214306TTG11GENICheterozygous69277024
109021491290214913TA14GENIChomozygous68165200
109021515490215155GA16GENIChomozygous68165203
109021696190216962TC13GENIChomozygous68165206
109021990690219907CA6GENIChomozygous68165210
109022031190220312GA21GENIChomozygous68165225
109022155490221555AC18GENICheterozygous68165228
109022178290221783AG10GENIChomozygous68165231
109022272390222724CT14GENIChomozygous68165237
109022302390223024AG6GENIChomozygous68165240
109022416190224162CT11GENIChomozygous68165246
109022417390224174AG10GENIChomozygous68165249
109022669690226697TA10GENIChomozygous68455206
109022764090227641CA31GENIChomozygous68455209
109023304490233045TC24GENIChomozygous68165277
109022287390222873G13GENICheterozygous69812064
109021808190218081T14GENIChomozygous69812063
109022758690227586CC23GENICheterozygous69812065