chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115356492115356493TC32GENIChomozygous112815342
4115356637115356638GC19GENIChomozygous112815344
4115357255115357256TG14GENIChomozygous112815346
4115357340115357341AG17GENIChomozygous112815348
4115357644115357645TA12GENICheterozygous112815350
4115357948115357949AT19GENIChomozygous112815352
4115359194115359195CG6GENIChomozygous126022332
4115359298115359299CT12GENIChomozygous126022333
4115363754115363755CT10GENIChomozygous112815356
4115364177115364178CT7GENIChomozygous112815358
4115366021115366022TC13GENIChomozygous112815360
4115366362115366363AG12GENIChomozygous112815362
4115366458115366459GA29GENIChomozygous112815364
4115366795115366796CT14GENIChomozygous112815366
4115367604115367605TC24GENIChomozygous112815368
4115367641115367642TC19GENIChomozygous112815370
4115368071115368072AG16GENIChomozygous112815372
4115368227115368228AG9GENIChomozygous112815374
4115368353115368354GC19GENIChomozygous112815376
4115369183115369184CG18GENIChomozygous112815382
4115369314115369315AG8GENIChomozygous112815384
4115369607115369608CT13GENIChomozygous112815386
4115369863115369864GA17GENIChomozygous112815388
4115370038115370039TG27GENIChomozygous112815390
4115371301115371302TC21GENIChomozygous112815392
4115371442115371443AC8GENIChomozygous112815394
4115371451115371452TG12GENIChomozygous112815396
4115372331115372332CG15GENIChomozygous112815398
4115375068115375069GA11GENIChomozygous112815400
4115375381115375382AC14GENIChomozygous112815402
4115375510115375511AG5GENIChomozygous113047972
4115377911115377912GC22GENIChomozygous112815406
4115381851115381852CG28GENIChomozygous112815412
4115382035115382036GA12GENIChomozygous112815414
4115382205115382206AT26GENIChomozygous112815416
4115382308115382309GA20GENIChomozygous112815418
4115383580115383581GA14GENIChomozygous112815420
4115383767115383768AG17GENIChomozygous112815422