chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18902355589023556GA67GENIChomozygous108884639
18902411089024111AG66GENICpossibly homozygous108884640
18902664289026643AC65GENIChomozygous120560802
18902938489029385TC59GENIChomozygous120560804
18902964389029644TA45GENIChomozygous108884643
18902995989029960GC48GENIChomozygous108884644
18903406389034064TC75GENIChomozygous109307760
18902924289029243G32GENIChomozygous131259956
18903403889034045GGCCTGT76GENIChomozygous131259957
18902971089029711AG41GENIChomozygous109307754
18903649389036494AG54GENICpossibly homozygous120560806
18903844089038441AT64GENIChomozygous120560808
18903864889038649GA80GENIChomozygous109307762
18904138989041389CACTGGT51GENIChomozygous131259958
18904139189041391AAC52GENIChomozygous131259959
18904214389042144G21GENIChomozygous127402169