chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38003180680031807CT29GENIChomozygous112132998
38003193580031936GA22GENIChomozygous111634955
38003350780033508AT33GENIChomozygous111634956
38003358280033583AG22GENIChomozygous111634957
38003409980034100TC16GENIChomozygous111634958
38003412980034130AT10GENIChomozygous112133000
38003465380034654TC17GENIChomozygous111634960
38003478680034787TA18GENIChomozygous111634961
38003493780034938AC19GENIChomozygous112133002
38003518080035181TC22GENIChomozygous111634962
38003643980036440CT25GENIChomozygous111634963
38003690180036902AG14GENIChomozygous112133004
38003717080037171TC27GENIChomozygous111634965
38003788480037885TA23GENIChomozygous111634966
38003870180038702GA25GENIChomozygous112133006
38003944380039444GA29GENIChomozygous112133008
38004026580040266TC26GENIChomozygous111634968
38004154280041543AG15GENIChomozygous111634971
38004258880042589AT30GENIChomozygous111634973
38004306180043062AT27GENICpossibly homozygous112133010
38004355780043558AC16GENICpossibly homozygous112133012
38004389480043895GA21GENIChomozygous112133014
38004390680043907CA21GENIChomozygous111634976
38004465980044660AG19GENIChomozygous111634978
38004495280044953AG28GENIChomozygous111634979
38004534780045348GA13GENICheterozygous111634980
38004538980045390AG28GENICheterozygous111634981
38004719980047200TA23GENIChomozygous111634983
38004809980048100TC17GENIChomozygous111634984
38004844980048450GA19GENIChomozygous111634985
38005051080050511CT28GENIChomozygous111634987
38005185080051851AG35GENIChomozygous111634988
38005186880051869TG37GENIChomozygous111634989
38005254480052545GC11GENIChomozygous111634991