chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121351511121351512AC15GENIChomozygous115858512
7121351659121351660AG19GENIChomozygous115858514
7121351666121351667GA18GENIChomozygous115858516
7121352112121352113AG18GENIChomozygous115858518
7121352821121352822AG18GENIChomozygous115858520
7121354414121354415CT20GENIChomozygous115858524
7121354892121354893AC14GENIChomozygous115858526
7121356568121356569GA18GENIChomozygous116409949
7121357005121357006TG18GENIChomozygous115858530
7121364825121364826GA28GENIChomozygous116409951
7121367352121367353TC26GENIChomozygous115858542
7121369373121369374AG18GENIChomozygous115858546
7121369747121369748CT35GENIChomozygous116409952
7121369953121369954GA31GENIChomozygous116409953
7121370431121370432TC26GENIChomozygous115858548
7121370678121370679CT29GENIChomozygous115858550
7121370951121370952GT31GENIChomozygous116409954
7121372869121372870TC20GENIChomozygous115858554
7121373043121373044TC30GENIChomozygous115858556
7121373775121373776GA32GENICpossibly homozygous116409955
7121374460121374461GA22GENIChomozygous116409956
7121374767121374768CT25GENIChomozygous115858560
7121374815121374816CA20GENIChomozygous116409957
7121375655121375656TC24GENIChomozygous116409958
7121376233121376234TC19GENIChomozygous115858562
7121378332121378333TC29GENIChomozygous115858566
7121381943121381944TC25GENIChomozygous115858572