chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2140709334140709335CCT13INTERGENICheterozygous59867593
2140709807140709809AT--22INTERGENIChomozygous59122353
2140710507140710508GGT26INTERGENICpossibly homozygous59867595
2140710508140710509GT34INTERGENICpossibly homozygous60145579
2140710518140710519GGT26INTERGENIChomozygous59122355
2140710637140710638GGT26INTERGENIChomozygous59122356
2140712538140712544TGTGTG------3INTERGENIChomozygous59867597
2140712965140712966TC38INTERGENIChomozygous59122364
2140714138140714139AC29INTERGENIChomozygous59867599
2140715720140715721CCAT15INTERGENICheterozygous59122376
2140715728140715730CA--15INTERGENICheterozygous59122378
2140715788140715789TTGC10INTERGENICheterozygous59122382
2140715789140715791AC--10INTERGENICheterozygous59867601
2140715811140715812AAT12INTERGENIChomozygous59122384
2140718755140718756CA17INTERGENICheterozygous59760941
2140720240140720241AC20INTERGENICpossibly homozygous59122394
2140720273140720274AC22INTERGENIChomozygous59122396
2140720309140720310AC14INTERGENIChomozygous59122398
2140720312140720314CA--13INTERGENIChomozygous59122400
2140722224140722225C-42INTERGENIChomozygous59867603
2140722934140722935CT28INTERGENICheterozygous59867605
2140723832140723833CA19INTERGENIChomozygous59867607
2140726497140726498GGTT10INTERGENICheterozygous59122406
2140726497140726498GGT10INTERGENICheterozygous59867609
2140726517140726518CT29INTERGENICheterozygous59122408
2140726692140726693GT56INTERGENIChomozygous59122412