chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110620512110620513GA25GENIChomozygous112292341
3110620795110620796CT29GENIChomozygous112292343
3110621260110621261CT25GENIChomozygous112292345
3110622393110622394CT21GENIChomozygous112292347
3110622982110622983AC19GENIChomozygous112003887
3110623216110623217CT27GENIChomozygous112138962
3110624496110624497GA19GENIChomozygous112003889
3110625631110625632TC26GENIChomozygous112003891
3110626964110626965CT28GENIChomozygous112292349
3110628152110628153TC25GENIChomozygous112003899
3110630082110630083GA20GENIChomozygous112292353
3110631947110631948GA22GENIChomozygous112292355
3110632367110632368AT27GENIChomozygous111673093
3110632368110632369GC27GENIChomozygous111673095
3110633139110633140CT19GENIChomozygous112292357
3110633253110633254GC24GENIChomozygous111673098
3110634584110634585GA32GENIChomozygous111673102
3110636109110636110TC12GENIChomozygous111673105
3110636137110636138GC8GENIChomozygous111673107
3110636553110636554TC16GENIChomozygous111673109
3110636841110636842AG31GENIChomozygous111673112
3110636918110636919AG29GENIChomozygous111673114
3110637465110637466AG23GENIChomozygous112138975
3110637822110637823GA15GENIChomozygous112292359
3110626881110626881ACCTGGT25GENIChomozygous130907821
3110631298110631299G17GENIChomozygous127918172
3110633583110633583ACA12GENIChomozygous127918173