chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115255608115255609AC47GENICpossibly homozygous112815031
4115258422115258423CA61GENICpossibly homozygous112815033
4115258594115258595TC55GENIChomozygous112815035
4115258679115258680GC62GENIChomozygous112815037
4115258687115258688GA62GENIChomozygous112815039
4115259797115259798TA46GENICheterozygous112815041
4115261930115261931AG55GENIChomozygous112815043
4115262141115262142GA38GENIChomozygous112815045
4115265585115265586AG45GENIChomozygous112815047
4115269353115269354CT45GENIChomozygous112815049
4115270254115270255GA49GENIChomozygous112815051
4115270764115270765AC52GENIChomozygous112815053
4115271633115271634AC44GENIChomozygous112815055
4115272156115272157GA36GENICpossibly homozygous112815057
4115272999115273000AC46GENIChomozygous112815059
4115274349115274350CG47GENIChomozygous112815061
4115274808115274809TC53GENIChomozygous112815063
4115275324115275325GT53GENICpossibly homozygous112815065
4115275502115275503GT51GENIChomozygous112815067
4115275511115275512GA49GENICpossibly homozygous112815069
4115275873115275874GA28GENIChomozygous112815071
4115276334115276335TC31GENIChomozygous112815073
4115276963115276964CT45GENIChomozygous112815075
4115277336115277337GC40GENIChomozygous112815077