chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3153400282153400283CG23GENIChomozygous58237453
3153400556153400557CT21GENIChomozygous58237454
3153400879153400880TC18GENIChomozygous58237455
3153402368153402369TC26GENIChomozygous58237458
3153402387153402388GA23GENIChomozygous58237459
3153402715153402716TC23GENICpossibly homozygous58237460
3153403248153403249TC21GENIChomozygous58237461
3153403490153403491AG28GENIChomozygous58237462
3153404144153404145AG20GENIChomozygous58237463
3153404990153404991GA32GENIChomozygous58237464
3153405806153405807TA37GENIChomozygous58237465
3153407970153407971CG18GENICpossibly homozygous58237466
3153407977153407978CT26GENIChomozygous58237467
3153408633153408640TTTCTTT-------7GENIChomozygous58237468
3153408954153408955CCT7GENIChomozygous58237472
3153408998153408999GA14GENIChomozygous58237474
3153409013153409014TC14GENIChomozygous58237475
3153410218153410219TTA37GENIChomozygous57741627
3153410930153410931TTTCACTGGGGCTGAGTAGATCAACTGAAGCTTTGTTTCACATAGTTTATACTCGGCCATAAGTA41GENIChomozygous58628653
3153411128153411129T-35GENIChomozygous57741629
3153412161153412162AG19GENIChomozygous58237476
3153413040153413041GA35GENIChomozygous58237477
3153413049153413053TTTT----20GENICheterozygous58628654
3153413050153413053TTT---20GENICheterozygous58564642
3153413573153413574GGTT23GENICheterozygous58237480
3153413573153413574GGTTT23GENICheterozygous58628655
3153414053153414054GA23GENIChomozygous58237481
3153414668153414670GA--22GENIChomozygous58237482
3153415197153415198AG30GENIChomozygous58237483
3153415246153415247CCAA25GENIChomozygous58237484
3153415741153415811TTGTATAAATACTATATATGAAATATATGGTATCTTGTTCCCCAGAAAAATCAGTGGGTTGTGGGTTGGG----------------------------------------------------------------------2GENIChomozygous58628656
3153416049153416050CCTTTT17GENIChomozygous58628657
3153416273153416274GGT29GENIChomozygous58237485
3153417890153417891GA28GENIChomozygous58237486