chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71269310012693101CT14GENIChomozygous115570348
71269396012693961CT12GENICpossibly homozygous115570349
71269425912694260AG20GENIChomozygous115570350
71269466912694670AG22GENIChomozygous115570351
71269524312695244TG16GENICpossibly homozygous115570352
71269541412695415TC11GENIChomozygous115570353
71269557712695578TA9GENIChomozygous115570354
71269560612695607CT9GENIChomozygous115570355
71269613012696131AG15GENIChomozygous115570356
71269642012696421TC18GENIChomozygous115570357
71269667812696679GA29GENIChomozygous115570358
71269692912696930TC41GENICheterozygous116114749
71269703812697039AG30GENIChomozygous115570359
71269749912697500AG23GENIChomozygous115570360
71269839712698398GA9GENIChomozygous115570361
71269848412698485TC8GENIChomozygous115570362
71269859812698599TC6GENIChomozygous115570363
71269879612698797GA22GENICpossibly homozygous115570364
71269891512698916TG18GENIChomozygous115570365
71269926912699270GA26GENIChomozygous115570366
71269938912699390GA15GENIChomozygous115570367
71269981612699817CT15GENIChomozygous115570368
71270052012700521CT20GENIChomozygous115570369
71270113812701139TC19GENIChomozygous115570370
71270250012702501AG21GENIChomozygous115570371
71270267412702675AG25GENIChomozygous115570372
71270268012702681TC25GENIChomozygous115570373
71270289912702900GA21GENIChomozygous115570374
71270309612703097TC18GENIChomozygous115570375
71270344212703443CT10GENIChomozygous115570376
71270477812704779CT24GENIChomozygous115570377
71270530912705310TC21GENIChomozygous115570378
71270647912706480CT22GENIChomozygous115570379
71270649912706500CT22GENIChomozygous115570380
71270665312706654CA28GENIChomozygous115570381
71270755512707556GA30GENIChomozygous115570382