chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
39390921893909219AG29GENIChomozygous111958108
39391067693910677AG25GENIChomozygous111958110
39391239193912392AC27GENIChomozygous111958114
39391252393912524AG16GENIChomozygous111958116
39391258493912585TC23GENIChomozygous111958118
39391756593917566AG7GENIChomozygous112134398
39391784493917845AT14GENIChomozygous119981767
39391214893912149GA29GENIChomozygous119981758
39391350493913505GA21GENIChomozygous119981760
39391674793916748GT22GENIChomozygous119981762
39391444193914445AGAC16GENIChomozygous131626456
39391779893917798T13GENIChomozygous131626457
39391799893917999CT14GENIChomozygous119981769
39391852493918525GA12GENIChomozygous119981771
39391969593919696TC27GENIChomozygous111958126
39392187193921872GT22GENIChomozygous111958128
39392703493927035TC18GENIChomozygous119981773
39392726693927267GA28GENIChomozygous119981775
39392738293927383CA23GENIChomozygous119981777
39392739493927395CT21GENIChomozygous112134408
39392768793927688GA18GENIChomozygous111958140
39392772893927729GA23GENIChomozygous119981779
39392874593928746CG18GENIChomozygous112134409
39392899293928993CT31GENIChomozygous112134410
39392902593929026AG31GENIChomozygous119981781
39392929993929300CT29GENICpossibly homozygous119981783
39392943293929433GA26GENIChomozygous112134411
39392944393929444CT26GENIChomozygous119981785
39392966893929669CT22GENIChomozygous112134412
39392975693929757AG30GENIChomozygous112134414
39393026793930268CT25GENIChomozygous119981787
39393035093930350G11GENICpossibly homozygous131626458
39393188793931888AC18GENIChomozygous119683476
39391832993918351ACACACACACACACACACACAT6GENIChomozygous133473512
39392027193920272CT20GENIChomozygous120018089
39393119593931196GT20GENIChomozygous120018090
39392049293920493CG22GENIChomozygous120101636
39392608593926085T11GENIChomozygous127909731
39393165793931658TA19GENIChomozygous119683470
39393165893931659AG19GENIChomozygous119683472