chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1223054168223054169TC12GENIChomozygous668397353
1223055722223055723AG8GENICheterozygous668397354
1223055729223055730TC9GENIChomozygous668397355
1223056450223056451CT8GENICheterozygous668397356
1223056525223056526G-17GENICpossibly homozygous768130605
1223056934223056935AG7GENICpossibly homozygous668397357
1223057104223057105TG9GENICheterozygous668397358
1223057341223057342GGGGT2GENICheterozygous768130606
1223057371223057393TGGTTTCTGAAAAGGGCTGTAC----------------------2GENIChomozygous768130607
1223057563223057566GGT---2GENICheterozygous768130608
1223057564223057566GT--2GENICheterozygous768130609
1223058902223058903TG16GENIChomozygous668397359
1223060667223060668GA20GENICpossibly homozygous668397360
1223061220223061221AAG4GENIChomozygous768130610
1223061321223061322AG11GENICheterozygous668397361
1223061586223061628TGGGAGGGACCCCTGGACAAATGGTGTGGCCCTGGTTTAGGA------------------------------------------1GENIChomozygous768130611
1223062949223062950AG21GENIChomozygous668397362
1223063185223063186CG18GENIChomozygous668397363
1223063512223063513AG11GENICheterozygous668397364
1223063612223063614CC--7GENIChomozygous768130612
1223063859223063860TC7GENIChomozygous668397365
1223063915223063916AG11GENIChomozygous668397366
1223064745223064746CA22GENICpossibly homozygous668397367
1223065081223065082TA10GENICpossibly homozygous668397368
1223065511223065512GA8GENIChomozygous668397369
1223065917223065918GA14GENICpossibly homozygous668397370
1223066136223066137C-21GENICheterozygous768130613
1223066194223066195TG15GENIChomozygous668397371
1223066755223066756AG7GENIChomozygous668397372
1223066789223066790GA18GENIChomozygous668397373
1223066996223066997TC20GENICpossibly homozygous668397374
1223067233223067234CT25GENIChomozygous668397375
1223067659223067660AG17GENIChomozygous668397376