chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123346315123346316AG20GENIChomozygous54089675
7123346726123346727AATT13GENICheterozygous55632206
7123346728123346729T-13GENICheterozygous55132554
7123347010123347011AATGCG22GENIChomozygous54089676
7123347360123347361CT30GENIChomozygous54089677
7123347384123347385AG34GENIChomozygous54089678
7123347940123347941GGCTGGGCCATGT23GENIChomozygous54089679
7123348246123348247GGA8GENICheterozygous55097126
7123348247123348248A-8GENICheterozygous54089680
7123348814123348815TA30GENIChomozygous54089681
7123348859123348860TC46GENIChomozygous54089682
7123349207123349208TC30GENIChomozygous54089683
7123349443123349444GT34GENIChomozygous54089684
7123350138123350139GA26GENIChomozygous54089685
7123350418123350419CT23GENIChomozygous54089686
7123350874123350875CT32GENIChomozygous54089687
7123350877123350878AT30GENIChomozygous54089688
7123351156123351157CA48GENIChomozygous54089689
7123351653123351654GA42GENIChomozygous54089690
7123352497123352498TC36GENIChomozygous54089691
7123356125123356126GC15GENIChomozygous54089703
7123356450123356451AG33GENIChomozygous54089704
7123357098123357099GA39GENIChomozygous54089705
7123357255123357256TC24GENIChomozygous54089706
7123357410123357411GA32GENIChomozygous54089707
7123357440123357441CT31GENIChomozygous54089708
7123357681123357682CCT23GENIChomozygous54089709
7123357682123357683GA23GENIChomozygous55097130
7123357684123357685GA24GENIChomozygous55097132
7123358237123358238GA26GENIChomozygous54089710
7123359043123359044TC25GENIChomozygous54089711
7123359169123359170TC27GENIChomozygous54089712
7123359192123359193GA26GENIChomozygous54089713
7123359357123359358GA14GENIChomozygous54089714
7123359647123359648CCAAA12GENICheterozygous55097134
7123359780123359781AG30GENIChomozygous54089715