chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7131967494131967495GC18GENIChomozygous69139889
7131968785131968786TC14GENIChomozygous69139893
7131969781131969782AG16GENIChomozygous69139898
7131970287131970288GA17GENIChomozygous69139900
7131970691131970692GA6GENIChomozygous69139909
7131971092131971093GA10GENIChomozygous69139913
7131973621131973622TA22GENIChomozygous69139920
7131976230131976231GA8GENIChomozygous69139928
7131976351131976352AG29GENIChomozygous69139932
7131977104131977105GA16GENIChomozygous69139936
7131977129131977130AG14GENIChomozygous69139940
7131977362131977362A12GENICheterozygous70806508
7131969455131969455AC25GENICheterozygous70806499
7131970547131970548G23GENICheterozygous70052115
7131969632131969632G6GENIChomozygous70806502
7131972174131972174A22GENICheterozygous70806505
7131975662131975663CA16GENICheterozygous69862893
7131977797131977798CT10GENIChomozygous69139947
7131979444131979445AC4GENIChomozygous69139951
7131979822131979823GC11GENIChomozygous69139957
7131980524131980525GA5GENIChomozygous69139962
7131980993131980994TC14GENIChomozygous69139968
7131981061131981062TC10GENIChomozygous69139972
7131981216131981217A7GENIChomozygous70052121
7131981399131981400TC24GENIChomozygous69139980
7131981980131981981CT16GENIChomozygous69139983
7131982332131982333AG6GENIChomozygous69139987
7131983124131983127TTA5GENIChomozygous70635229
7131983962131983963TC16GENIChomozygous69139995
7131984731131984732CT15GENIChomozygous69139999
7131985013131985014TC5GENIChomozygous69140003
7131985162131985163TG8GENIChomozygous69140007