chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7131967494131967495GC22GENIChomozygous69139889
7131968785131968786TC15GENIChomozygous69139893
7131969781131969782AG20GENIChomozygous69139898
7131970287131970288GA19GENIChomozygous69139900
7131970691131970692GA23GENIChomozygous69139909
7131971092131971093GA19GENIChomozygous69139913
7131972405131972406TC11GENIChomozygous69139916
7131973621131973622TA27GENIChomozygous69139920
7131976210131976211GA28GENIChomozygous69139924
7131976230131976231GA27GENIChomozygous69139928
7131976351131976352AG14GENIChomozygous69139932
7131977104131977105GA18GENIChomozygous69139936
7131977129131977130AG18GENIChomozygous69139940
7131977573131977574AG8GENIChomozygous69139943
7131977797131977798CT14GENIChomozygous69139947
7131979444131979445AC8GENIChomozygous69139951
7131979670131979671TC9GENIChomozygous69139955
7131979822131979823GC4GENIChomozygous69139957
7131980524131980525GA1GENIChomozygous69139962
7131980993131980994TC9GENIChomozygous69139968
7131981061131981062TC4GENICheterozygous69139972
7131981399131981400TC7GENIChomozygous69139980
7131981980131981981CT21GENIChomozygous69139983
7131982332131982333AG10GENIChomozygous69139987
7131983111131983112TC22GENIChomozygous69139991
7131983962131983963TC30GENIChomozygous69139995
7131984731131984732CT25GENIChomozygous69139999
7131985013131985014TC15GENICpossibly homozygous69140003
7131985162131985163TG11GENIChomozygous69140007