chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133286569133286570AT52GENIChomozygous113306428
4133286970133286971AG51GENIChomozygous112832478
4133287184133287185TG53GENIChomozygous112832479
4133287420133287421AG51GENIChomozygous112832480
4133288712133288713AG66GENIChomozygous112832483
4133289375133289376GA33GENIChomozygous113306430
4133290376133290377GC14GENICpossibly homozygous112832485
4133290380133290381GC13GENIChomozygous112832486
4133291435133291435T45GENIChomozygous128079966
4133293382133293383CT52GENIChomozygous113306433
4133293509133293509T31GENIChomozygous131642117
4133288158133288159GA57GENIChomozygous119411261
4133290108133290109TC57GENIChomozygous119411262
4133291349133291350TC43GENIChomozygous119411263
4133292578133292579AT49GENIChomozygous119411264
4133290360133290361GC12GENICheterozygous130946628
4133290372133290373GC14GENICpossibly homozygous130946629
4133290368133290369GC14GENICpossibly homozygous131645728
4133290707133290711ACCT45GENIChomozygous131642114
4133290819133290823CTTT42GENIChomozygous131642115
4133291656133291656AA40GENIChomozygous131642116
4133294478133294479CT36GENIChomozygous119411265
4133294677133294678A44GENICpossibly homozygous131642118
4133294869133294870CT57GENIChomozygous113306434
4133295704133295705GA62GENIChomozygous112832488
4133296455133296459ATTT26GENIChomozygous131642119
4133296502133296503CT44GENICpossibly homozygous131645729
4133293885133293885TTTTTTTTTTTTTC10GENICheterozygous133131797
4133314781133314783AG7GENIChomozygous131642120
4133314814133314815GT20GENIChomozygous112832489
4133314824133314825CT24GENIChomozygous112832490
4133315669133315670AT3GENIChomozygous126023278
4133316804133316805GA47GENIChomozygous113385208
4133316950133316950ACTGACAT53GENIChomozygous128079968
4133317122133317123GC49GENIChomozygous112832492
4133320646133320647T34GENIChomozygous131642121