chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122234628122234629GA28GENIChomozygous115860340
7122250577122250578GT15GENICpossibly homozygous115860342
7122257716122257717TG25GENICheterozygous115860344
7122266012122266013GA21GENIChomozygous115860346
7122267472122267473CT31GENIChomozygous115860348
7122270035122270036TC25GENICheterozygous116082035
7122270064122270065TA31GENICheterozygous116082036
7122270066122270067AG31GENICheterozygous116082037
7122270071122270072TA32GENICheterozygous116082038
7122270081122270082AC33GENICheterozygous116082039
7122270085122270086TC33GENICheterozygous116082040
7122270094122270095TA32GENICheterozygous116082041
7122270096122270097TG33GENICheterozygous116082042
7122270103122270104AG30GENICheterozygous116376903
7122270106122270107CT31GENICheterozygous116082043
7122270114122270115GC32GENICheterozygous116376905
7122270119122270120CT31GENICheterozygous116376907
7122273177122273178AG13GENIChomozygous115860350
7122302396122302397AG21GENIChomozygous115860352
7122312981122312982CA16GENIChomozygous115860354
7122313196122313197TA24GENICheterozygous115860356
7122342957122342958CT17GENICheterozygous116376909
7122346584122346585AG14GENIChomozygous115860358
7122347648122347649CA11GENIChomozygous115860360
7122347812122347813CA16GENIChomozygous115860362
7122349972122349973CA7GENIChomozygous115860364
7122349975122349976CG7GENIChomozygous115860366
7122364947122364948AG7GENIChomozygous115860368
7122378672122378673AG17GENIChomozygous116082063
7122378673122378674AT17GENIChomozygous116082064
7122378674122378675AC17GENIChomozygous116082065
7122401914122401915AC27GENICpossibly homozygous115860376