chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150689860150689861A-16GENIChomozygous55794303
5150691202150691203AG43GENIChomozygous55794307
5150691959150691960TC17GENIChomozygous55794308
5150692638150692639TC26GENIChomozygous55794311
5150693001150693002AG43GENIChomozygous55794312
5150693275150693276AG24GENIChomozygous55794313
5150693616150693617TC19GENIChomozygous55794314
5150693673150693674AG24GENIChomozygous55794315
5150693730150693731TC27GENIChomozygous55794316
5150694600150694604CTCT----5GENIChomozygous55794317
5150695158150695159AG35GENIChomozygous55794318
5150695273150695274TC20GENIChomozygous55794319
5150695422150695423TTACACACACACACACAC9GENICheterozygous56570221
5150695708150695709CT23GENIChomozygous55794321
5150696202150696203TC28GENIChomozygous55794322
5150696582150696583GC27GENIChomozygous55794323
5150696706150696707CG28GENIChomozygous55794324
5150696929150696930AATG27GENIChomozygous55794332
5150703488150703489GT35GENIChomozygous55794338
5150692483150692484GGA11GENIChomozygous56554445
5150695422150695423TTACACACACACAC9GENICheterozygous56460608
5150696694150696695CCTGTGTGTCTGTGTG31GENIChomozygous56460609
5150698104150698105AAT20GENIChomozygous55794333
5150698648150698649CT31GENIChomozygous55794334
5150700645150700646GA30GENIChomozygous55794335
5150702261150702262GT25GENIChomozygous55794336
5150703291150703292GT23GENIChomozygous55794337
5150705160150705161TTA14GENIChomozygous55794339
5150705308150705309CCA13GENICheterozygous55794341
5150705460150705462AA--16GENIChomozygous55924122
5150712090150712091CCCAGGCTCTGCCG24GENIChomozygous55794342
5150713327150713328GGTGAATGAT26GENIChomozygous55794343
5150720787150720788CT24GENIChomozygous55794347
5150722133150722134A-10GENIChomozygous55794348
5150722147150722148A-14GENIChomozygous55794349