chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71202249012022491AG25GENICpossibly homozygous53789960
71202301312023014AG6GENICheterozygous53789961
71202323612023237CT11GENICheterozygous53789962
71202331112023312AG8GENICheterozygous53789963
71202373012023731TG11GENICpossibly homozygous53789964
71202389112023892AG15GENIChomozygous53789965
71202411412024115TC17GENICpossibly homozygous53789966
71202447012024471GA12GENICheterozygous53789967
71202481612024817TC11GENICheterozygous53789968
71202481712024818GA11GENICheterozygous53789969
71202561912025620TG10GENIChomozygous53789973
71202586512025866GA9GENIChomozygous53789974
71202590712025908CT16GENICpossibly homozygous53789975
71202595912025960CT9GENICheterozygous53789976
71202631512026316AG23GENIChomozygous53789977
71202641912026420TC18GENIChomozygous53789978
71202748112027482GA14GENICpossibly homozygous53789980
71202812912028130CA17GENICpossibly homozygous53789981
71202839512028396AG7GENIChomozygous53789982
71202879412028795CA11GENIChomozygous53789983
71202966912029670TC7GENIChomozygous53789984
71203201712032018TG5GENIChomozygous56141819
71203218412032185GGGGCAGGTACCT2GENIChomozygous56141822
71203497712034978CA23GENICpossibly homozygous56141824
71203532112035322CT2GENIChomozygous53789994
71203544412035445CT5GENICheterozygous53789996
71203554112035542TC10GENICpossibly homozygous53789997
71203608612036087TC22GENIChomozygous53789998
71203765112037652GC4GENIChomozygous53790002
71203767512037676AG1GENIChomozygous53790003
71203797312037974CA17GENICpossibly homozygous53790004
71203852512038526CA1GENIChomozygous54954696
71203852612038527AT1GENIChomozygous54181720
71203862812038629TC9GENICheterozygous56141826
71203881512038816AT12GENIChomozygous53790010
71203956012039561TC22GENIChomozygous53790011
71203965812039659AG16GENICpossibly homozygous53790012
71204042212040423CT6GENIChomozygous56141829
71204058712040588TA4GENIChomozygous53790015
71204139712041398AG21GENIChomozygous53790016