chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2251805412251805414TT3GENIChomozygous127764245
2251805414251805415TG4GENIChomozygous120132169
2251805417251805417G5GENIChomozygous127764246
2251805418251805419CA5GENIChomozygous120132170
2251805954251805955AG10GENIChomozygous125611493
2251807756251807757AT13GENIChomozygous127841643
2251807757251807758AT13GENIChomozygous127841644
2251807997251807998GA28GENICpossibly homozygous110386370
2251808065251808066AT32GENICpossibly homozygous110386372
2251808278251808279T53GENIChomozygous127764247
2251808593251808594GA42GENIChomozygous110386374
2251808633251808634TA33GENIChomozygous110386376
2251808931251808932AC35GENIChomozygous110386378
2251809050251809051CA50GENIChomozygous110386380
2251809668251809669TC47GENIChomozygous110386382
2251809983251809989TGCTAT58GENIChomozygous127764248
2251810800251810801GC47GENIChomozygous110386384
2251811234251811235CG17GENIChomozygous110386386
2251812062251812063AG41GENIChomozygous110386388
2251813099251813100AG46GENIChomozygous110386390
2251813146251813147GA44GENIChomozygous110386392
2251813360251813360A43GENIChomozygous127764249
2251813558251813559AT59GENIChomozygous110386394
2251813895251813896GA45GENIChomozygous110386396
2251814165251814166TC50GENIChomozygous110386398
2251814194251814195AC46GENICpossibly homozygous110386400