chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150685716150685717TC19GENIChomozygous114348914
5150686278150686279CT15GENIChomozygous114348916
5150687272150687273CT16GENIChomozygous114348918
5150689377150689378AG16GENIChomozygous114348920
5150690664150690665GA24GENIChomozygous114348922
5150690906150690907TC15GENIChomozygous114348924
5150691339150691340GA14GENIChomozygous114348926
5150691388150691389CT12GENIChomozygous114348928
5150691430150691431AG15GENIChomozygous114540368
5150692118150692119TA13GENIChomozygous114348932
5150692120150692121GC13GENIChomozygous114348934
5150692122150692123TC13GENIChomozygous114348936
5150694736150694737TC20GENIChomozygous114540378
5150695315150695316CG20GENIChomozygous114540380
5150695760150695761CT20GENIChomozygous114348944
5150699625150699626GA7GENIChomozygous114348950
5150699631150699632TC7GENIChomozygous114348952
5150700387150700387GCACATCG30GENIChomozygous131652033
5150701466150701467TC21GENIChomozygous114348956
5150701897150702017CCAGAAGCTAGCATTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCC14GENICpossibly homozygous131652034
5150703071150703072AC31GENIChomozygous114348958
5150688837150688838TC14GENIChomozygous119021232
5150692348150692349AG30GENIChomozygous119021234
5150697663150697664GA20GENIChomozygous119021236
5150699962150699963CT21GENIChomozygous119021238
5150700269150700270GA24GENIChomozygous119021240
5150702419150702420CT34GENIChomozygous119021242
5150693526150693526GAT20GENIChomozygous132845502
5150694258150694259T13GENIChomozygous132845503
5150696850150696851G7GENIChomozygous134089358
5150699719150699720GT20GENIChomozygous132850018