chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3153400282153400283CG20GENIChomozygous58237453
3153400556153400557CT37GENIChomozygous58237454
3153400879153400880TC36GENIChomozygous58237455
3153402368153402369TC32GENIChomozygous58237458
3153402387153402388GA34GENIChomozygous58237459
3153402715153402716TC43GENIChomozygous58237460
3153403248153403249TC55GENIChomozygous58237461
3153403490153403491AG38GENIChomozygous58237462
3153404144153404145AG40GENIChomozygous58237463
3153404990153404991GA31GENIChomozygous58237464
3153405806153405807TA26GENIChomozygous58237465
3153407970153407971CG18GENICheterozygous58237466
3153407970153407971C-18GENICheterozygous58697233
3153407977153407978CT24GENIChomozygous58237467
3153408633153408640TTTCTTT-------8GENICpossibly homozygous58237468
3153408954153408955CCT8GENIChomozygous58237472
3153408998153408999GA10GENIChomozygous58237474
3153409013153409014TC12GENIChomozygous58237475
3153410218153410219TTA31GENIChomozygous57741627
3153410930153410931TTTCACTGGGGCTGAGTAGATCAACTGAAGCTTTGTTTCACATAGTTTATACTCGGCCATAAGTA72GENIChomozygous58628653
3153411128153411129T-33GENIChomozygous57741629
3153412161153412162AG25GENIChomozygous58237476
3153413040153413041GA20GENIChomozygous58237477
3153413050153413053TTT---18GENICheterozygous58564642
3153413573153413574GGTT21GENIChomozygous58237480
3153414053153414054GA32GENIChomozygous58237481
3153414668153414670GA--32GENIChomozygous58237482
3153415197153415198AG27GENIChomozygous58237483
3153415246153415247CCAA33GENIChomozygous58237484
3153415741153415811TTGTATAAATACTATATATGAAATATATGGTATCTTGTTCCCCAGAAAAATCAGTGGGTTGTGGGTTGGG----------------------------------------------------------------------8GENIChomozygous58628656
3153416049153416050CCTTTT13GENIChomozygous58628657
3153416273153416274GGT22GENIChomozygous58237485
3153417890153417891GA37GENIChomozygous58237486