chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106709067967090680AG7GENIChomozygous51909284
106709497067094974TTGT----2GENIChomozygous51680305
106709760867097609GGT2GENICheterozygous51480486
106709849067098491TC20GENIChomozygous51680314
106709862067098621GGT4GENIChomozygous51480487
106709950467099505C-1GENIChomozygous51680316
106710303267103033CT3GENIChomozygous51909293
106710313967103140GT5GENICheterozygous51909295
106710421567104216CA18GENICheterozygous51909297
106710744467107445GT2GENICheterozygous51480492
106710754567107546TG4GENIChomozygous51480506
106710755467107555CA5GENIChomozygous51480507
106710755567107556TA5GENIChomozygous51480508
106710756067107561TA6GENIChomozygous51480509
106710756267107563CG6GENIChomozygous51480510
106710796667107967G-1GENIChomozygous51909301
106710971867109719TC11GENIChomozygous51909303
106711979867119799AC14GENICpossibly homozygous51909305
106712158067121581AATGATTGATT1GENIChomozygous51480511
106712329467123295GA10GENICpossibly homozygous51909309
106712826767128268GA17GENIChomozygous51909313
106712979367129794AG18GENIChomozygous51680410
106713009867130099AG29GENICpossibly homozygous51909315
106713204267132043AATT6GENIChomozygous51680412
106709777467097780TTTTCA------2GENIChomozygous52320444
106710935067109355GGTTC-----1GENIChomozygous52320446