chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7835887978358880AG7GENICpossibly homozygous45153198
X7835933478359335CT8GENIChomozygous45153199
X7836295678362957A-12GENIChomozygous45153201
X7836544878365449GA2GENICheterozygous45153202
X7836681478366815AT5GENICheterozygous45153203
X7836681578366816AT5GENICheterozygous45153204
X7837024078370241C-5GENIChomozygous45153206
X7837058078370581TC9GENIChomozygous45153207
X7837238078372381CCTGTA8GENICheterozygous45479012
X7837898978378990TC2GENIChomozygous45153218
X7838042478380425GGAC3GENIChomozygous45153219
X7838521278385213TC2GENIChomozygous45153220
X7838660578386606AT11GENIChomozygous45153221
X7838759478387595TA6GENICheterozygous45153222
X7838780978387810CT4GENIChomozygous45153223
X7839165378391654CT2GENIChomozygous45153226
X7839169378391694AC4GENIChomozygous45153227
X7839177678391777TA6GENIChomozygous45153228
X7839341278393413TC11GENIChomozygous45153229
X7839349478393495AC3GENIChomozygous45153230
X7839367078393671GT6GENIChomozygous45153231
X7839394378393944AAT2GENIChomozygous45153232
X7839753078397531AC8GENIChomozygous45153233
X7840226678402267TTCCTCCTC1GENIChomozygous45513589
X7839781778397818CT3GENIChomozygous45153234
X7840103978401040AT13GENIChomozygous45153235
X7840183178401832TC15GENIChomozygous45153236
X7840263778402638CT8GENIChomozygous45153242
X7840400178404002T-3GENIChomozygous45153243
X7840641078406411GA6GENIChomozygous45153244
X7840781978407820TG1GENIChomozygous45153245
X7840793178407932GA10GENIChomozygous45153246