chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7835887978358880AG14GENIChomozygous45153198
X7835933478359335CT13GENIChomozygous45153199
X7836056478360565TTA4GENIChomozygous45153200
X7836295678362957A-11GENIChomozygous45153201
X7836544878365449GA9GENIChomozygous45153202
X7836681478366815AT5GENIChomozygous45153203
X7836681578366816AT5GENIChomozygous45153204
X7836934678369348AT--5GENIChomozygous45153205
X7837024078370241C-6GENIChomozygous45153206
X7837058078370581TC11GENIChomozygous45153207
X7837304178373042GGT1GENIChomozygous45153208
X7837898978378990TC6GENIChomozygous45153218
X7838042478380425GGAC6GENIChomozygous45153219
X7838521278385213TC10GENIChomozygous45153220
X7838625178386259TATATATG--------1GENIChomozygous45548278
X7838660578386606AT7GENIChomozygous45153221
X7838759478387595TA8GENIChomozygous45153222
X7838780978387810CT8GENIChomozygous45153223
X7838814178388142AG5GENIChomozygous45153224
X7839165378391654CT7GENIChomozygous45153226
X7839169378391694AC6GENIChomozygous45153227
X7839177678391777TA9GENIChomozygous45153228
X7839341278393413TC11GENIChomozygous45153229
X7839349478393495AC11GENIChomozygous45153230
X7839367078393671GT18GENIChomozygous45153231
X7839394378393944AAT16GENIChomozygous45153232
X7839753078397531AC12GENIChomozygous45153233
X7839781778397818CT7GENIChomozygous45153234
X7840103978401040AT11GENIChomozygous45153235
X7840183178401832TC13GENIChomozygous45153236
X7840234078402341TC4GENIChomozygous45153240
X7840234178402342TC5GENIChomozygous45153241
X7839032578390326A-6GENIChomozygous45513587
X7840226678402267TTCCTCCTC11GENIChomozygous45513589
X7840235978402363TCCT----4GENIChomozygous45513591
X7840263778402638CT6GENIChomozygous45153242
X7840400178404002T-13GENICpossibly homozygous45153243
X7840641078406411GA13GENIChomozygous45153244
X7840781978407820TG17GENIChomozygous45153245
X7840793178407932GA10GENIChomozygous45153246