chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77051766170517662AT7GENICpossibly homozygous53956712
77051856870518569TC6INTERGENIChomozygous53956714
77051999270519993TC25INTERGENIChomozygous53956721
77052181370521814AG17GENICpossibly homozygous53956729
77052260870522609GT21GENIChomozygous53956731
77052292070522924CTAA----1GENIChomozygous53956733
77052306270523063CT13GENIChomozygous54445323
77052843270528433AAGTT3GENIChomozygous54445325
77052879770528798CT13GENIChomozygous54445327
77052926170529262AG17GENICheterozygous54445333
77052936570529366AG14GENICpossibly homozygous54445335
77053014870530149GC9GENICheterozygous54445337
77053112970531130AG10GENIChomozygous54445339
77053121970531220AG10GENIChomozygous54445342
77053186570531866A-24GENIChomozygous54445344
77053192770531928TG17GENICpossibly homozygous54445346
77053274570532746CT16GENICheterozygous54445348
77053460670534607CT5GENIChomozygous54445349
77053487770534878TG14GENIChomozygous54445351
77053583970535840GT4GENIChomozygous53956743
77053584370535844AT2GENIChomozygous54445353
77053900170539002GA11GENIChomozygous54445355
77053973870539739GA16GENIChomozygous54445357
77054075370540754AG12GENIChomozygous54445359
77054078970540790AAC8GENIChomozygous53956753
77054411070544111GC15GENIChomozygous53956761
77054490270544903G-1GENIChomozygous54445364
77054571470545734ACACACACACACACACACAC--------------------1GENIChomozygous54445366
77055062270550623TC12GENIChomozygous53956765
77055092870550929GA11GENIChomozygous54445370
77055200370552004GT12GENIChomozygous54445372
77055258570552586GA11GENIChomozygous53956769