chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115664174115664175A-13GENICheterozygous52826543
8115664738115664739TG41GENIChomozygous52826544
8115664873115664874AAGT22GENICpossibly homozygous52826545
8115664940115664941T-20GENICpossibly homozygous52826546
8115665958115665959GGT25GENICheterozygous52826547
8115665958115665959GGTT25GENICpossibly homozygous52826548
8115667352115667353AG33GENIChomozygous52826549
8115667354115667355GGA30GENIChomozygous52826550
8115671235115671236A-11GENIChomozygous52826551
8115671348115671349CG46GENIChomozygous52826552
8115671402115671403CT45GENIChomozygous52826553
8115674266115674267CCT48GENIChomozygous52826554
8115674491115674492GC43GENIChomozygous52826555
8115674526115674527TG46GENIChomozygous52826556