chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3153400282153400283CG24GENIChomozygous58237453
3153400556153400557CT12GENIChomozygous58237454
3153400879153400880TC16GENIChomozygous58237455
3153402368153402369TC23GENIChomozygous58237458
3153402387153402388GA23GENIChomozygous58237459
3153402715153402716TC36GENIChomozygous58237460
3153403248153403249TC26GENIChomozygous58237461
3153403490153403491AG23GENIChomozygous58237462
3153404144153404145AG33GENIChomozygous58237463
3153404990153404991GA29GENIChomozygous58237464
3153405806153405807TA18GENIChomozygous58237465
3153407970153407971CG12GENICheterozygous58237466
3153407970153407971C-12GENICheterozygous58697233
3153407977153407978CT18GENIChomozygous58237467
3153408633153408640TTTCTTT-------6GENIChomozygous58237468
3153408962153408963TTTG13GENICpossibly homozygous58237473
3153408998153408999GA15GENIChomozygous58237474
3153409013153409014TC23GENIChomozygous58237475
3153410930153410931TTTCACTGGGGCTGAGTAGATCAACTGAAGCTTTGTTTCACATAGTTTATACTCGGCCATAAGTA33GENIChomozygous58628653
3153412161153412162AG29GENIChomozygous58237476
3153413040153413041GA17GENIChomozygous58237477
3153413049153413053TTTT----12GENICheterozygous58628654
3153413573153413574GGTT10GENIChomozygous58237480
3153414053153414054GA33GENIChomozygous58237481
3153414668153414670GA--17GENIChomozygous58237482
3153415197153415198AG29GENIChomozygous58237483
3153415246153415247CCAA27GENIChomozygous58237484
3153416049153416050CCTTTT9GENIChomozygous58628657
3153416273153416274GGT14GENIChomozygous58237485
3153417890153417891GA23GENIChomozygous58237486
3153413050153413053TTT---12GENICheterozygous58564642
3153410218153410219TTA23GENIChomozygous57741627
3153411128153411129T-30GENIChomozygous57741629