chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5148432610148432611AC23GENIChomozygous114049249
5148434471148434472CG32GENIChomozygous114049251
5148435139148435140TC22GENICpossibly homozygous114049253
5148435143148435144TC21GENICpossibly homozygous114049255
5148435147148435148TC22GENICpossibly homozygous114049257
5148438171148438172TC28GENICpossibly homozygous114049259
5148438230148438231TG27GENICpossibly homozygous114049261
5148438731148438732GA21GENIChomozygous114049263
5148438887148438888TC19GENIChomozygous114049265
5148438940148438941AG26GENIChomozygous114049267
5148439173148439174CT25GENIChomozygous114049269
5148439641148439642CG26GENIChomozygous114049283
5148439654148439655GA25GENIChomozygous114049284
5148440152148440153CT19GENIChomozygous118846609
5148440153148440154TC21GENIChomozygous118846610
5148440206148440207CG20GENIChomozygous114049286
5148440589148440590TC17GENIChomozygous114049288
5148442812148442813AG13GENIChomozygous114049292
5148442951148442952AG7GENIChomozygous114049294
5148443022148443023TC5GENIChomozygous118937159
5148443564148443565CT12GENIChomozygous114049298
5148443965148443966CT18GENIChomozygous114049300