chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77051766170517662AT3GENIChomozygous53956712
77051856870518569TC16INTERGENIChomozygous53956714
77051952570519526GC2INTERGENIChomozygous53956717
77051952770519528AAG1INTERGENIChomozygous53956719
77051999270519993TC21INTERGENICpossibly homozygous53956721
77052181370521814AG17GENIChomozygous53956729
77052260870522609GT25GENICpossibly homozygous53956731
77052292070522924CTAA----5GENIChomozygous53956733
77052306270523063CT15GENIChomozygous54445323
77052843270528433AAGTT8GENIChomozygous54445325
77052879770528798CT17GENIChomozygous54445327
77052926170529262AG11GENICheterozygous54445333
77052936570529366AG11GENIChomozygous54445335
77053014870530149GC16GENICpossibly homozygous54445337
77053112970531130AG12GENICpossibly homozygous54445339
77053121970531220AG21GENICpossibly homozygous54445342
77053186570531866A-22GENICpossibly homozygous54445344
77053192770531928TG27GENIChomozygous54445346
77053274570532746CT18GENIChomozygous54445348
77053459470534595A-2GENIChomozygous54572987
77053460670534607CT2GENIChomozygous54445349
77053487770534878TG10GENICpossibly homozygous54445351
77053583970535840GT4GENIChomozygous53956743
77053584370535844AT5GENIChomozygous54445353
77053900170539002GA25GENICheterozygous54445355
77053973870539739GA19GENICpossibly homozygous54445357
77054075370540754AG17GENICpossibly homozygous54445359
77054078970540790AAC6GENICheterozygous53956753
77054223470542235CG3GENIChomozygous54445360
77054411070544111GC23GENIChomozygous53956761
77054437470544375CA3GENIChomozygous54445362
77054490270544903G-2GENICheterozygous54445364
77054571470545734ACACACACACACACACACAC--------------------2GENICheterozygous54445366
77055062270550623TC17GENICheterozygous53956765
77055092870550929GA8GENIChomozygous54445370
77055200370552004GT17GENICpossibly homozygous54445372
77055258570552586GA23GENIChomozygous53956769