chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7131967494131967495GC25GENIChomozygous69139889
7131968785131968786TC20GENIChomozygous69139893
7131969781131969782AG18GENIChomozygous69139898
7131970287131970288GA21GENIChomozygous69139900
7131970691131970692GA25GENIChomozygous69139909
7131971092131971093GA16GENIChomozygous69139913
7131972405131972406TC13GENIChomozygous69139916
7131973621131973622TA36GENIChomozygous69139920
7131976210131976211GA38GENIChomozygous69139924
7131976230131976231GA34GENIChomozygous69139928
7131976351131976352AG33GENIChomozygous69139932
7131977104131977105GA22GENIChomozygous69139936
7131977129131977130AG18GENIChomozygous69139940
7131977573131977574AG17GENIChomozygous69139943
7131977797131977798CT32GENIChomozygous69139947
7131979444131979445AC22GENIChomozygous69139951
7131979670131979671TC7GENIChomozygous69139955
7131979822131979823GC20GENIChomozygous69139957
7131980524131980525GA17GENIChomozygous69139962
7131980768131980769AC7GENIChomozygous69139965
7131980993131980994TC12GENIChomozygous69139968
7131981061131981062TC18GENIChomozygous69139972
7131981077131981078CT17GENIChomozygous69139976
7131981399131981400TC18GENIChomozygous69139980
7131981980131981981CT28GENIChomozygous69139983
7131982332131982333AG26GENIChomozygous69139987
7131984731131984732CT33GENIChomozygous69139999
7131983111131983112TC43GENIChomozygous69139991
7131983962131983963TC34GENIChomozygous69139995
7131985013131985014TC26GENICpossibly homozygous69140003
7131985162131985163TG18GENIChomozygous69140007