chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5158121012158121012C11GENIChomozygous128263230
5158121024158121025C10GENIChomozygous128263231
5158121033158121033CC9GENIChomozygous128263232
5158121057158121058G8GENIChomozygous128263233
5158121916158121917G34GENIChomozygous128263234
5158121940158121940T29GENIChomozygous128263235
5158121944158121945G26GENIChomozygous128263236
5158121948158121948GGT26GENIChomozygous128263237
5158121950158121951A27GENIChomozygous128263238
5158121952158121953CA28GENIChomozygous118847144
5158123137158123139AT55GENIChomozygous131652841
5158123525158123526TC46GENICpossibly homozygous114070895
5158123659158123660AG50GENIChomozygous114070896
5158125991158125992AG57GENIChomozygous114070897
5158127264158127265C28GENIChomozygous128263241
5158127318158127319CG36GENIChomozygous133402296
5158127493158127494AG50GENIChomozygous114070902
5158129116158129229AAGACCTATGAGGTCGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAACACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAAAAAAAAAAAAA48GENIChomozygous128263242
5158129275158129276TC46GENIChomozygous114070904
5158129406158129407GT68GENICpossibly homozygous114070905
5158130388158130389GA63GENIChomozygous114070907
5158130857158130858CG44GENIChomozygous114070908
5158130978158130991GTCCTGTTAGAGT38GENIChomozygous131652842
5158131205158131206AG70GENIChomozygous114070909
5158132557158132558GA45GENIChomozygous114070913
5158132729158132730TC56GENIChomozygous114070914
5158133538158133539CT67GENIChomozygous114070915
5158122901158122902CT55GENIChomozygous119186578
5158124824158124825GA65GENIChomozygous119186580
5158125248158125249TG58GENIChomozygous119186581
5158134034158134035GA60GENIChomozygous119186582
5158127322158127323CG34GENIChomozygous134940507
5158131025158131026AC53GENIChomozygous126314211