chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156466955156466956TC1GENIChomozygous648677213
5156467036156467037CT1GENIChomozygous648677214
5156467062156467063AG2GENIChomozygous648677215
5156467249156467250CT3GENIChomozygous648677216
5156468792156468793A-25GENIChomozygous756278753
5156469168156469169GA28GENIChomozygous648677217
5156469329156469330AG21GENIChomozygous648677218
5156469343156469344GT22GENIChomozygous648677219
5156469557156469558AC17GENIChomozygous648677220
5156469704156469705AG15GENIChomozygous648677221
5156469734156469735AG14GENIChomozygous648677222
5156469760156469761AG19GENIChomozygous648677223
5156469881156469882CT7GENIChomozygous648677224
5156469901156469902TTTTTTC7GENICpossibly homozygous756278754
5156470006156470007AG17GENIChomozygous648677225
5156470324156470325AG15GENIChomozygous648677226
5156470972156470973GA30GENIChomozygous648677227
5156471176156471177AC29GENIChomozygous648677228
5156471550156471551GA25GENIChomozygous648677229
5156471721156471722CA18GENICpossibly homozygous648677230