chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
996789799678980AG6GENIChomozygous126495945
996795169679517CT22GENIChomozygous126495946
996800139680014CT15GENIChomozygous126495947
996805839680584TC21GENIChomozygous126495948
996811519681152GA8GENIChomozygous126495949
996811649681165AC7GENIChomozygous126495950
996811899681190CT17GENIChomozygous126495951
996812159681216GA13GENIChomozygous126495952
996813769681377TA7GENIChomozygous126495953
996816269681627CT22GENIChomozygous126495954
996816579681658TA23GENIChomozygous126495955
996817779681778GA19GENIChomozygous126495956
996818829681883GA16GENIChomozygous126495957
996819499681950CT20GENIChomozygous126495958
996824509682451GT15GENIChomozygous126495959
996824769682477AG11GENIChomozygous126495960
996825569682557TC20GENIChomozygous126495961
996828469682847CT4GENICheterozygous126495962
996830699683070CT20GENIChomozygous126495963
996835029683503AG23GENIChomozygous126495964
996835399683540TG10GENIChomozygous126495965
996845599684560TC7GENIChomozygous126495966
996846099684610CT24GENIChomozygous126495967
996857329685733GA16GENIChomozygous126495968
996857709685771TG10GENIChomozygous126495969
996859009685901CT26GENIChomozygous126495970
996859679685968TC26GENIChomozygous126495971
996861669686167AG21GENIChomozygous126495972
996863759686376CT21GENIChomozygous126495973
996868369686837CT18GENIChomozygous126495974
996871969687197GA18GENIChomozygous126495975
996872599687260CT16GENIChomozygous126495976
996873999687400TC9GENIChomozygous126495977
996879299687930AG20GENIChomozygous126495978
996880399688040TC17GENIChomozygous126495979
996882889688289CT18GENIChomozygous126495980