chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109145316891453169TC19GENIChomozygous938901019
109145325291453253GT16GENIChomozygous938901020
109145464991454650GA13GENIChomozygous938901021
109145504291455043CG14GENIChomozygous938901022
109145519991455200AG22GENIChomozygous938901023
109145569791455698GA15GENIChomozygous938901024
109145643691456437CT21GENIChomozygous938901025
109145665891456659TC16GENIChomozygous938901026
109145666291456663CA16GENIChomozygous938901027
109145998691459987TC24GENIChomozygous938901028
109146089391460894CT18GENIChomozygous938901029
109146107091461071AG15GENIChomozygous938901030
109146109791461098GA10GENIChomozygous938901031
109146202891462029TC24GENIChomozygous938901032
109146213791462138AG21GENIChomozygous938901033
109146258791462588CT25GENIChomozygous938901034
109146273791462738GA29GENIChomozygous938901035
109146334991463350AG25GENIChomozygous938901036
109146355891463559AC14GENIChomozygous938901037
109146712991467130TC14GENIChomozygous938901038
109146851291468513AG24GENIChomozygous938901039
109146889991468900AG23GENIChomozygous938901040
109146911791469118CA27GENIChomozygous938901041
109147070591470706CT21GENIChomozygous938901042
109147123691471237CT33GENIChomozygous938901043
109147154091471541CT26GENIChomozygous938901044
109147297791472978CT29GENIChomozygous938901045
109147335491473355TG24GENIChomozygous938901046
109147596891475969AT29GENIChomozygous938901047
109148319691483197TC24GENIChomozygous938901048
109148327291483273TG18GENIChomozygous938901049
109148530091485301CT27GENIChomozygous938901050
109148898891488989TC29GENIChomozygous938901051
109149013591490136CA31GENIChomozygous938901052
109149048491490485CG20GENIChomozygous938901053
109149447991494480GA24GENIChomozygous938901054
109149585291495853TC13GENIChomozygous938901055
109149626091496261AT20GENIChomozygous938901056
109149809391498094TC15GENIChomozygous938901057