chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187143910187143911GA35GENIChomozygous120377949
2187143920187143925GCCGC33GENIChomozygous131297862
2187143926187143927CA32GENIChomozygous120377950
2187143928187143928A31GENIChomozygous131297863
2187143936187143937GA29GENIChomozygous120377951
2187143974187143975TC20GENIChomozygous120393690
2187143992187143993C17GENICheterozygous130253158
2187144026187144026T22GENIChomozygous131297864
2187144404187144405AC51GENIChomozygous120377952
2187145125187145126AG38GENICpossibly homozygous120377953
2187145795187145796GA41GENIChomozygous120377954
2187145968187145969TC53GENIChomozygous120377955
2187146154187146155CT46GENIChomozygous120377956
2187146225187146226TC49GENIChomozygous120377957
2187147700187147701CT49GENIChomozygous120377958
2187150174187150175TC40GENIChomozygous110166971
2187147311187147312AC44GENICpossibly homozygous110166967
2187148150187148151GA36GENIChomozygous110166968
2187148907187148908AG50GENIChomozygous110166969
2187149621187149622AG22GENIChomozygous110166970
2187150330187150331TC43GENIChomozygous110166972
2187150707187150708AG17GENIChomozygous110166973
2187150711187150712AG17GENIChomozygous111146540
2187151567187151568GA63GENIChomozygous110166975
2187152289187152290GA49GENIChomozygous120377959
2187152461187152462AG48GENIChomozygous110166977
2187153004187153005TC37GENIChomozygous110166978
2187153114187153115TC38GENIChomozygous110166979
2187154184187154185AG49GENIChomozygous110166982
2187154789187154790TA34GENICheterozygous134926699
2187154798187154799TA34GENICheterozygous134926700
2187154803187154804TA35GENICheterozygous134926701
2187155908187155909GA45GENIChomozygous110166985
2187156064187156065TC52GENIChomozygous110166986