chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4107923084107923085CT4GENICheterozygous126081010
4107947403107947404GA4GENIChomozygous126021756
4107986346107986347CG16GENICheterozygous126040476
4108056752108056753AC18GENIChomozygous119346612
4108167959108167960AT3GENICheterozygous126081011
4108273465108273466CA4GENIChomozygous126081012
4108314507108314508CT7GENICheterozygous126081013
4108382055108382056CT3GENICheterozygous126081014
4108407122108407123GT20GENIChomozygous126021759
4108456014108456015AT12GENIChomozygous126021760
4108508993108508994GT21GENIChomozygous119346618
4108512651108512652TA20GENIChomozygous126021761
4108512768108512769GA26GENIChomozygous126021762
4108515951108515952TA12GENIChomozygous126021763
4108515964108515965GT9GENIChomozygous126021764
4108515980108515981TG9GENIChomozygous126021765
4108516028108516029CT4GENIChomozygous126040482
4108516030108516031TC6GENIChomozygous126040483
4108516036108516037GC9GENIChomozygous126040484
4108516052108516053GC18GENIChomozygous126021766
4108516108108516109GT21GENIChomozygous126021767
4108522427108522428AT3GENICheterozygous126081015
4108550667108550668TG19GENIChomozygous126021768
4108555055108555056GT7GENIChomozygous126081016
4108559908108559909CA22GENIChomozygous126021769
4108559973108559974CG19GENIChomozygous126021770
4108560024108560025TC24GENIChomozygous126021771
4108560063108560064CT5GENIChomozygous126021772
4108569383108569384TG6GENICheterozygous126081017
4108653169108653170TA9GENICheterozygous126052482
4108653294108653295GT10GENICheterozygous126021775
4108685804108685805CT19GENIChomozygous126021778
4108807972108807973CA4GENIChomozygous126081018
4108818495108818496GC14GENIChomozygous112806738
4108818554108818555CA10GENIChomozygous126052486
4108850375108850376GA3GENICheterozygous119459250
4108880896108880897AC17GENIChomozygous126081019
4108980925108980926TC21GENIChomozygous112806772
4109039483109039484GC4GENIChomozygous126081020