chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1216946341694635GT14GENIChomozygous115577911
1216946481694650GC15GENIChomozygous128948639
1216947731694774C34GENIChomozygous128948640
1217147181714719A22GENIChomozygous128948656
1217147211714722A22GENIChomozygous128948657
1217165901716591AT31GENIChomozygous115232434
1217147571714758GT18GENIChomozygous118286903
1217118301711832AC27GENICheterozygous130405000
1217146941714694C27GENIChomozygous130405001
1217365851736585A55GENIChomozygous128948672
1217366471736648TA54GENIChomozygous115232500
1217366601736662AT48GENIChomozygous128948673
1217366751736675A49GENIChomozygous128948674
1217367221736723T52GENIChomozygous128948675
1217367531736753A51GENIChomozygous128948676
1217367881736789C48GENIChomozygous128948677
1217368301736831T44GENIChomozygous128948678
1217368361736837C45GENIChomozygous128948679
1217368721736873C40GENIChomozygous128948680
1217368901736891G43GENIChomozygous128948681
1217369221736923T42GENIChomozygous128948682
1217370501737051CA50GENIChomozygous115357111
1217370781737079T54GENIChomozygous128948686
1217370201737021T55GENIChomozygous128948683
1217370641737064G51GENIChomozygous128948684
1217370651737065C52GENIChomozygous128948685
1217370821737082C55GENIChomozygous128948687
1217371481737148A55GENIChomozygous128948688
1217530151753016AC21GENICheterozygous129004961
1217530201753021AC22GENICheterozygous129004962
1217530251753026AC20GENICheterozygous129004963
1217530311753032GC20GENICheterozygous129004964
1217633331763334A48GENICheterozygous130405002
1217790371779038GA45GENICheterozygous118234835
1217790451779046TC46GENICheterozygous118234836
1217790491779050GC47GENICheterozygous118234837
1217790631779064TG45GENICheterozygous118234839
1217790661779067CA45GENICheterozygous118234840
1217792751779276CG50GENICheterozygous118334575
1217792791779280CT51GENICheterozygous118334576
1217793021779303AT44GENICheterozygous118334577
1217794171779418AC50GENICheterozygous118234842
1217822671782268CG48GENICheterozygous130688410