chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75497866154978662GT3INTERGENIChomozygous54195890
75498486354984864AC22INTERGENICheterozygous53929002
75498488654984887GA30INTERGENICheterozygous54395826
75498492654984927CT41INTERGENICheterozygous53929004
75498494454984945GT38INTERGENICheterozygous53929006
75498516354985164AT14INTERGENICheterozygous54395828
75498516554985166AT14INTERGENICheterozygous53929008
75498519454985195G-4INTERGENIChomozygous53929010
75498521354985214CA14INTERGENICheterozygous54395830
75498537154985372TG8INTERGENICheterozygous54195891
75498645054986451TTTGTGTGTG20INTERGENICheterozygous53929016
75500449955004500CT14GENIChomozygous53929077
75500453155004532C-7GENIChomozygous54195894
75502466955024670GGCTTGCTA2GENICheterozygous53929092
75503346455033465GA37GENICheterozygous53929094
75504738355047387AAAC----38GENICheterozygous53929096
75505317255053173CCT19GENIChomozygous53929097
75505317555053176C-18GENICpossibly homozygous53929098
75507391155073912GA60GENICheterozygous54736013
75508211955082120CT44GENIChomozygous54795905
75509650555096507AA--8GENIChomozygous53929101
75509653555096539AACG----2GENIChomozygous53929102
75509654555096546A-1GENIChomozygous53929103
75509654855096555AGACAAA-------1GENIChomozygous53929105
75510602855106029GGT25GENIChomozygous53929107
75510994755109948GC64GENICheterozygous53929109
75510998855109989AG58GENICheterozygous53929111
75511004155110042TC44GENICheterozygous54195897
75511010755110108TTTC10GENIChomozygous53929112
75513380255133803TA73GENICheterozygous54195898
75514598455145985CT71GENICheterozygous53929118
75514919855149199GT37GENICheterozygous53929121
75515260055152601C-21GENIChomozygous53929123
75511083955110840TG66GENIChomozygous54822802
75511844655118447TG29GENICheterozygous54822804