chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136110536136110537GC14GENIChomozygous624743178
4136110720136110721GA18GENIChomozygous624743179
4136110835136110836AC23GENICpossibly homozygous624743180
4136110909136110910AG15GENIChomozygous624743181
4136110954136110955CT9GENICheterozygous624743182
4136110960136110961CG11GENICheterozygous624743183
4136111031136111032TC13GENIChomozygous624743184
4136111098136111099CT15GENIChomozygous624743185
4136111170136111171GA16GENIChomozygous624743186
4136111227136111228TA15GENICpossibly homozygous624743187
4136111299136111300AC17GENIChomozygous624743188
4136111384136111385CG14GENICpossibly homozygous624743189
4136111468136111469AC27GENIChomozygous624743190
4136111652136111653AG10GENIChomozygous624743191
4136111961136111962CT24GENICpossibly homozygous624743192
4136112220136112221CG11GENIChomozygous624743193
4136112376136112377TTCC4GENICheterozygous740610288
4136112628136112629GA24GENICheterozygous624743194
4136112694136112695AG20GENICpossibly homozygous624743195
4136112778136112779AG22GENIChomozygous624743196
4136113093136113094GA15GENIChomozygous624743197
4136113250136113251AG12GENIChomozygous624743198
4136113414136113416GG--4GENIChomozygous740610289
4136113431136113432G-1GENIChomozygous740610290
4136113433136113434G-1GENIChomozygous740610291
4136113453136113454GGTA1GENIChomozygous740610292
4136113461136113462AATG1GENIChomozygous740610293
4136113541136113542AC1GENIChomozygous624743199
4136113579136113580AC7GENIChomozygous624743200
4136113750136113751TG10GENICpossibly homozygous624743201
4136113770136113771CG12GENIChomozygous624743202
4136113933136113934TG12GENICpossibly homozygous624743203
4136113975136113976AC11GENIChomozygous624743204
4136114069136114070GA13GENIChomozygous624743205
4136114208136114209GA21GENIChomozygous624743206
4136114614136114615GA12GENIChomozygous624743207