chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14114130099114130100AG26GENIChomozygous113558459
14114139803114139804GA37GENIChomozygous113558461
14114141618114141619CG16GENIChomozygous113558463
14114141680114141681CT34GENIChomozygous113558465
14114143872114143873TC45GENICheterozygous113699777
14114143954114143955AG34GENICheterozygous113558467
14114143988114143989AT30GENICheterozygous113558469
14114143995114143996TG27GENICheterozygous113558471
14114148216114148217TC22GENIChomozygous113558475
14114148982114148983GC25GENIChomozygous113699779
14114149745114149746TG31GENIChomozygous113558477
14114149795114149796CA25GENIChomozygous113558479
14114157086114157087AG32GENIChomozygous113558481
14114157363114157364CA29GENIChomozygous113558483
14114159356114159357AT39GENIChomozygous113558485
14114159488114159489CT23GENIChomozygous113558487
14114160023114160024TC18GENIChomozygous113558489
14114160181114160182CT18GENICheterozygous113699781
14114163015114163016GT20GENIChomozygous113558491
14114163566114163567TA41GENIChomozygous113558493
14114164276114164277AG35GENIChomozygous113558495
14114172727114172728TC29GENIChomozygous113558497