chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2154520833154520834AG66GENIChomozygous110768550
2154521257154521258CT53GENIChomozygous110768552
2154521832154521833GA68GENIChomozygous110065339
2154523478154523479GA55GENIChomozygous110065341
2154524636154524637CG47GENIChomozygous110768554
2154524703154524704CT43GENIChomozygous110768556
2154524706154524710AGCC42GENIChomozygous131293349
2154525945154525946AC64GENICpossibly homozygous110768557
2154526379154526380TC53GENIChomozygous110768559
2154527269154527270CT60GENIChomozygous110768561
2154527527154527528AG48GENIChomozygous110768563
2154527538154527542TAAG48GENIChomozygous131293350
2154530139154530139T38GENICpossibly homozygous131293351
2154530652154530653AG77GENIChomozygous110768565
2154530754154530755CA58GENIChomozygous110768566
2154531941154531941CATG67GENICpossibly homozygous131293352
2154533107154533108G49GENIChomozygous131293353
2154534203154534204CG61GENIChomozygous110065352
2154534830154534831CT52GENIChomozygous110768568
2154535023154535024GA42GENIChomozygous110768570
2154535779154535780CT71GENIChomozygous110768574
2154535813154535814CT71GENIChomozygous110768576
2154536206154536207GA46GENIChomozygous110768578
2154536260154536261GA44GENIChomozygous110768580
2154536781154536782TA31GENIChomozygous120150928
2154523295154523295G56GENIChomozygous127693029
2154524350154524351GT25GENIChomozygous110977559
2154530967154530968GT26GENICheterozygous130637950
2154533108154533109TA50GENIChomozygous120150925
2154536777154536778TA21GENICpossibly homozygous120150926
2154536779154536780TA32GENIChomozygous120150927
2154537477154537478GC63GENIChomozygous110768582
2154537696154537696C48GENIChomozygous131293356
2154537701154537701C51GENIChomozygous131293357
2154538184154538185TC58GENIChomozygous110065359
2154537696154537697GA48GENIChomozygous131313646