chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2251805412251805414TT1GENIChomozygous127764245
2251805414251805415TG1GENIChomozygous120132169
2251805417251805417G1GENIChomozygous127764246
2251805418251805419CA2GENIChomozygous120132170
2251805954251805955AG2GENIChomozygous125611493
2251807756251807757AT7GENIChomozygous127841643
2251807757251807758AT7GENIChomozygous127841644
2251808278251808279T25GENIChomozygous127764247
2251808931251808932AC17GENIChomozygous110386378
2251807997251807998GA15GENIChomozygous110386370
2251808065251808066AT21GENIChomozygous110386372
2251808593251808594GA34GENIChomozygous110386374
2251808633251808634TA30GENIChomozygous110386376
2251809050251809051CA31GENIChomozygous110386380
2251809668251809669TC27GENIChomozygous110386382
2251809983251809989TGCTAT27GENIChomozygous127764248
2251810800251810801GC28GENIChomozygous110386384
2251811234251811235CG13GENIChomozygous110386386
2251812062251812063AG28GENIChomozygous110386388
2251813099251813100AG36GENIChomozygous110386390
2251813146251813147GA34GENIChomozygous110386392
2251813360251813360A28GENIChomozygous127764249
2251813558251813559AT32GENIChomozygous110386394
2251813895251813896GA31GENIChomozygous110386396
2251814165251814166TC33GENIChomozygous110386398
2251814194251814195AC26GENIChomozygous110386400