chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5176666017176666018TG11GENICpossibly homozygous56101077
5176666260176666277TACCCTACACACTTGTA-----------------1GENIChomozygous56466747
5176666621176666622CT23GENIChomozygous56101079
5176668903176668904AAC8GENIChomozygous56101080
5176668904176668905AAAAC9GENIChomozygous56101084
5176669702176669703GT23GENICpossibly homozygous56101086
5176670049176670051AA--1GENIChomozygous56555564
5176670662176670663AG28GENICpossibly homozygous56101090
5176671481176671482TG16GENIChomozygous56101092
5176671763176671789CTAGGCCTCCTCATTAGAGTGCAGGG--------------------------4GENIChomozygous56101094
5176672493176672494GA12GENICpossibly homozygous56101096
5176673260176673261CT16GENIChomozygous55849359
5176673929176673930AG15GENIChomozygous55849361
5176674660176674661AG18GENIChomozygous55849363
5176675836176675837AG15GENICheterozygous55849365
5176677733176677734CA9GENIChomozygous55849379
5176678214176678215GGCTA15GENICpossibly homozygous56101102
5176679322176679323GA9GENICpossibly homozygous56101106
5176679781176679782AG10GENICpossibly homozygous55849387
5176680639176680640TC24GENIChomozygous55849389
5176681188176681189G-6GENICheterozygous56101108
5176681530176681531GA20GENIChomozygous56101110
5176682518176682519AC22GENIChomozygous56101112
5176682608176682609GA18GENIChomozygous56101114
5176683087176683088TA14GENICpossibly homozygous56101116
5176683464176683465AG26GENIChomozygous55849393
5176684518176684519CG26GENICpossibly homozygous56101119