chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2140543254140543255TG20GENIChomozygous110035142
2140543514140543515AG10GENICheterozygous125589138
2140548101140548102GA18GENIChomozygous110035149
2140548932140548933TG19GENIChomozygous110035151
2140549496140549497AG17GENIChomozygous110035152
2140550800140550801CT14GENIChomozygous110035156
2140551269140551270CG7GENIChomozygous110035157
2140551283140551284CT13GENICheterozygous110035159
2140551310140551311CG20GENIChomozygous110035160
2140551563140551564TC25GENIChomozygous110035164
2140552190140552191AG16GENIChomozygous110035165
2140545872140545873TC6GENICheterozygous125762352
2140548649140548650CT9GENICheterozygous125762353
2140547137140547138TA17GENIChomozygous120445259
2140547641140547642CT14GENIChomozygous120445260
2140549973140549974AG18GENIChomozygous120445261