chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274649890274649891AG29GENIChomozygous797275790
1274650039274650040GC36GENIChomozygous797275791
1274650282274650283GA18GENIChomozygous797275792
1274650699274650700CT26GENIChomozygous797275793
1274650826274650827AG44GENICpossibly homozygous797275794
1274651771274651772CG21GENIChomozygous797275795
1274652276274652277CT34GENIChomozygous797275796
1274652501274652502GC33GENIChomozygous797275797
1274654008274654009AG39GENIChomozygous797275798
1274656146274656147TA35GENICpossibly homozygous797275799
1274656149274656150TA37GENICpossibly homozygous797275800
1274657810274657811TC37GENIChomozygous797275801
1274658000274658001CT29GENICpossibly homozygous797275802
1274658404274658405TC28GENIChomozygous797275803
1274659241274659242CG25GENIChomozygous797275804
1274660606274660607CT19GENIChomozygous797275805
1274661596274661597GT22GENIChomozygous797275806
1274663202274663203CT34GENIChomozygous797275807