chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166934682166934683CT32INTERGENIChomozygous60932454
1166934927166934928CG32INTERGENIChomozygous60932455
1166935044166935045AT29INTERGENIChomozygous60932456
1166935059166935060GA29INTERGENIChomozygous60932457
1166935091166935092CA34INTERGENIChomozygous60932458
1166935113166935114TTA38INTERGENIChomozygous60932459
1166935134166935135GA43INTERGENIChomozygous60932460
1166935354166935355CT24INTERGENIChomozygous60932461
1166935379166935380TC28INTERGENIChomozygous60932462
1166935451166935452GGA39INTERGENIChomozygous60932464
1166935492166935493CT37INTERGENIChomozygous60932465
1166935597166935598GT43INTERGENIChomozygous60932466
1166935627166935628CT41INTERGENIChomozygous60932467
1166935699166935711TGAATGAATGAA------------14INTERGENIChomozygous62352771
1166935758166935759AG20INTERGENIChomozygous60932470
1166935815166935816GC27INTERGENIChomozygous60932471
1166935877166935878CT41INTERGENIChomozygous60932472
1166935922166935923CG37INTERGENIChomozygous60932473
1166936053166936054GA34INTERGENIChomozygous60932474
1166936401166936402TG29INTERGENIChomozygous60932475
1166937051166937052CT30INTERGENIChomozygous60932476
1166938002166938003GA21INTERGENIChomozygous60932477
1166938281166938282TC6INTERGENIChomozygous60932478
1166938425166938426TG10INTERGENIChomozygous60932479
1166938486166938490TGTG----11INTERGENICheterozygous60932480
1166938488166938490TG--11INTERGENICheterozygous60932481
1166939112166939113CT33INTERGENIChomozygous60932482
1166940450166940451AT24INTERGENIChomozygous60932483
1166940576166940577GA33INTERGENIChomozygous60932484
1166942380166942381CT35INTERGENIChomozygous60932485
1166943396166943397AT37INTERGENIChomozygous60932486