chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7131967494131967495GC31GENIChomozygous69139889
7131968785131968786TC22GENIChomozygous69139893
7131969781131969782AG22GENIChomozygous69139898
7131970287131970288GA16GENIChomozygous69139900
7131970691131970692GA25GENIChomozygous69139909
7131971092131971093GA24GENIChomozygous69139913
7131972405131972406TC15GENIChomozygous69139916
7131973621131973622TA30GENIChomozygous69139920
7131976210131976211GA41GENIChomozygous69139924
7131976230131976231GA37GENIChomozygous69139928
7131976351131976352AG20GENIChomozygous69139932
7131977104131977105GA24GENIChomozygous69139936
7131977129131977130AG22GENIChomozygous69139940
7131977573131977574AG21GENIChomozygous69139943
7131977613131977614CG27GENICheterozygous81978729
7131977797131977798CT27GENIChomozygous69139947
7131979444131979445AC13GENIChomozygous69139951
7131979670131979671TC10GENIChomozygous69139955
7131979822131979823GC18GENIChomozygous69139957
7131980524131980525GA7GENIChomozygous69139962
7131980768131980769AC4GENIChomozygous69139965
7131980993131980994TC24GENIChomozygous69139968
7131981061131981062TC21GENIChomozygous69139972
7131981077131981078CT14GENIChomozygous69139976
7131981399131981400TC20GENIChomozygous69139980
7131981980131981981CT29GENIChomozygous69139983
7131982332131982333AG26GENIChomozygous69139987
7131983111131983112TC25GENIChomozygous69139991
7131983962131983963TC30GENIChomozygous69139995
7131984731131984732CT39GENIChomozygous69139999
7131985013131985014TC20GENICheterozygous69140003
7131985162131985163TG28GENIChomozygous69140007