chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
114489084544890851AAAAAA------8INTERGENICheterozygous50762173
114489336044893361TTA7INTERGENICheterozygous50762233
114489401444894015GA65INTERGENICheterozygous50762237
114489409644894097TG37INTERGENICheterozygous50762241
114489411444894115CA36INTERGENICheterozygous50879789
114489411744894118GT37INTERGENICheterozygous50762244
114490013044900134ATCT----13INTERGENICpossibly homozygous50949508
114490231644902317AATATG2INTERGENICheterozygous50879792
114490473144904732TTA5INTERGENIChomozygous50762349
114494153844941540GA--22INTERGENICheterozygous50762533
114495916944959170GT3INTERGENIChomozygous50762542
114496370744963708CG1INTERGENIChomozygous50762547
114496371344963714TA1INTERGENIChomozygous50762549
114496394844963949AG5INTERGENICheterozygous50879802
114496510544965111AGAGAG------7INTERGENICheterozygous50762585
114497097644970977A-16INTERGENIChomozygous50762627
114497098244970983CCA17INTERGENIChomozygous50762629
114497115944971160A-2INTERGENIChomozygous50762631
114497117844971179A-2INTERGENIChomozygous50762632
114497119744971198G-5INTERGENIChomozygous50762634
114497120044971201G-5INTERGENIChomozygous50762636
114497259844972599AT14INTERGENICheterozygous50988729
114497279044972791CT30INTERGENICheterozygous50762680
114497285044972851AC25INTERGENICheterozygous50762683
114498300744983008CA22INTERGENIChomozygous50762790
114498620844986209AAC16INTERGENIChomozygous50762817
114499691744996921AATG----14INTERGENICheterozygous50762862
114500354745003551GTGT----18INTERGENICheterozygous50762884
114500427645004277TG7INTERGENIChomozygous50762888
114500427745004278CG7INTERGENIChomozygous50762889
114500430545004306TG10INTERGENIChomozygous50762890
114500430745004308CT10INTERGENIChomozygous50762891