chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5176666017176666018TG32GENIChomozygous56101077
5176666260176666277TACCCTACACACTTGTA-----------------17GENIChomozygous56466747
5176666621176666622CT39GENIChomozygous56101079
5176668903176668904AAC28GENICpossibly homozygous56101080
5176668904176668905AAAAC28GENICpossibly homozygous56101084
5176669702176669703GT45GENIChomozygous56101086
5176670049176670051AA--17GENICheterozygous56555564
5176670050176670051A-17GENICheterozygous56466748
5176670335176670336GGA10GENICheterozygous56466749
5176670336176670341AAAAA-----10GENICpossibly homozygous56101088
5176670662176670663AG28GENIChomozygous56101090
5176671481176671482TG31GENIChomozygous56101092
5176671763176671789CTAGGCCTCCTCATTAGAGTGCAGGG--------------------------28GENIChomozygous56101094
5176672493176672494GA34GENIChomozygous56101096
5176673260176673261CT47GENIChomozygous55849359
5176673929176673930AG32GENIChomozygous55849361
5176674660176674661AG30GENIChomozygous55849363
5176675836176675837AG46GENIChomozygous55849365
5176676495176676496TTGCCAGGCA40GENIChomozygous56101098
5176676687176676695AAGGAGGA--------5GENIChomozygous55849367
5176676731176676738AAAAGGT-------17GENIChomozygous55849369
5176676770176676771A-20GENIChomozygous55849375
5176677733176677734CA34GENIChomozygous55849379
5176678214176678215GGCTA29GENIChomozygous56101102
5176678754176678755CCTT5GENIChomozygous56101104
5176678862176678863AT18GENIChomozygous55849385
5176679322176679323GA22GENIChomozygous56101106
5176679781176679782AG32GENIChomozygous55849387
5176680639176680640TC43GENIChomozygous55849389
5176681188176681189G-23GENIChomozygous56101108
5176681530176681531GA49GENIChomozygous56101110
5176682518176682519AC38GENIChomozygous56101112
5176682608176682609GA37GENIChomozygous56101114
5176683087176683088TA41GENIChomozygous56101116
5176683464176683465AG27GENIChomozygous55849393
5176683983176683984A-8GENIChomozygous56101118
5176684518176684519CG44GENIChomozygous56101119
5176685254176685255CT14GENIChomozygous56101121