chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117688687117688688AG41GENIChomozygous115847943
7117689117117689118GT17GENIChomozygous118258926
7117689911117689912CA41GENIChomozygous115847949
7117690326117690327CA36GENIChomozygous115847951
7117690388117690389TC39GENIChomozygous115847953
7117691535117691536CA43GENIChomozygous115847955
7117691541117691542CT45GENIChomozygous115847957
7117692538117692539GT41GENIChomozygous115847959
7117692677117692678CT48GENIChomozygous115847961
7117693000117693001TC55GENIChomozygous115847965
7117693023117693024TG60GENIChomozygous115847967
7117693844117693845GT41GENIChomozygous115847969
7117694013117694014TG36GENIChomozygous115847971
7117694816117694817TC47GENIChomozygous115847973
7117696183117696184AG47GENIChomozygous115847975
7117697243117697244AG57GENIChomozygous115847977
7117697852117697853GC59GENIChomozygous115847979
7117698209117698210CT35GENIChomozygous115847981
7117698224117698225GA38GENIChomozygous115847983
7117698395117698396CT45GENIChomozygous115847985
7117698957117698958AG24GENIChomozygous115847987
7117698994117698994G25GENIChomozygous128510680
7117689122117689123T17GENIChomozygous128510676
7117690354117690361AATAAAT39GENIChomozygous128510677
7117694044117694048GCTG30GENIChomozygous128510678
7117698989117698989C25GENIChomozygous128510679
7117689135117689136TC15GENIChomozygous116080610
7117695311117695314CTG43GENICheterozygous134012593
7117699037117699037T21GENIChomozygous128510681
7117699065117699065C16GENIChomozygous128510682
7117699311117699311G18GENICpossibly homozygous128510684
7117701313117701314CT47GENIChomozygous115847991
7117703041117703044CCG38GENIChomozygous128510685