chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144767426144767427TG26GENIChomozygous137645773
5144767431144767432C26GENIChomozygous137347702
5144767452144767453G27GENICheterozygous403161912
5144767446144767447T26GENICheterozygous403161909
5144767446144767447TC26GENIChomozygous403161910
5144767452144767453GC27GENIChomozygous403161911
5144767464144767465TC28GENIChomozygous137645774
5144769308144769310AT36GENIChomozygous137347704
5144769309144769310T36GENIChomozygous403161913
5144769309144769310TC36GENICheterozygous403161914
5144769317144769318G34GENICheterozygous403161915
5144769317144769318GC34GENICpossibly homozygous403161916
5144787188144787188T16GENICheterozygous144702728
5144773076144773078TC6GENICheterozygous141002844