chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5148434636148434637CT20GENIChomozygous114153735
5148435112148435113CA19GENICpossibly homozygous114153736
5148439466148439467GA6GENIChomozygous118913388
5148439641148439642CG13GENIChomozygous114049283
5148439654148439655GA10GENIChomozygous114049284
5148440589148440590TC12GENIChomozygous114049288
5148440663148440664GA8GENICpossibly homozygous114153738
5148441249148441250AG20GENIChomozygous114153739
5148441714148441715GA7GENIChomozygous114153740
5148441847148441848CT17GENIChomozygous114153741
5148442183148442184TC23GENIChomozygous114153742
5148442812148442813AG13GENIChomozygous114049292
5148442951148442952AG12GENIChomozygous114049294
5148443899148443900CT15GENIChomozygous114153745
5148443983148443984TC12GENIChomozygous114153746
5148444051148444052CT14GENIChomozygous114153747