chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1176872557176872559AC11GENICheterozygous140850921
1176872558176872559CT11GENICheterozygous403799315
1176872558176872559C11GENICheterozygous403799316
1176956113176956114G7GENICheterozygous403799319
1176956113176956114GC7GENICheterozygous403799320
1177015288177015289C9GENICheterozygous402974316
1177015288177015289CT9GENICheterozygous402974317
1177015331177015332A19GENICheterozygous403546396
1177015331177015332AT19GENICheterozygous403546397
1177017358177017359A10GENICheterozygous402974318
1177017358177017359AT10GENICheterozygous402974319
1177019895177019896G17GENICheterozygous402974320
1177019895177019896GC17GENICheterozygous402974321
1177023987177023988A16GENICheterozygous403972067
1177023987177023988AT16GENICheterozygous403972068
1177043965177043966T6GENICheterozygous402974322
1177043965177043966TA6GENICheterozygous402974323
1177043968177043969T6GENICheterozygous402974324
1177043968177043969TA6GENICheterozygous402974325
1177058582177058583CG9GENICheterozygous402974326
1177058582177058583C9GENIChomozygous402974327
1177126562177126563G11GENICpossibly homozygous402974328
1177126562177126563GC11GENICheterozygous402974329
1177134262177134263G12GENICheterozygous402974330
1177134262177134263GC12GENICheterozygous402974331
1177134817177134818A9GENICheterozygous402974332
1177134817177134818AT9GENICheterozygous402974333
1177134819177134820A9GENICheterozygous402974334
1177134819177134820AT9GENICheterozygous402974335