chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105731062657310627TG37GENIChomozygous117011619
105731131757311318CT18GENIChomozygous118083626
105731175257311753GA33GENIChomozygous116785309
105731266357312665CT20GENIChomozygous131094758
105731402957314030C13GENIChomozygous131094759
105731359357313594TC18GENIChomozygous117995041
105731868957318690TC19GENIChomozygous116785313
105732019957320200CT10GENICpossibly homozygous116785315
105732031757320318CT13GENIChomozygous116785317
105732045157320452AT14GENIChomozygous116890291
105732063857320639TG29GENIChomozygous117060262