chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116687137116687138AG60GENICpossibly homozygous116669925
8116687145116687146AC62GENICpossibly homozygous116669927
8116687608116687609TA62GENICpossibly homozygous117149181
8116689561116689562AG50GENIChomozygous116669929
8116689917116689918GA52GENIChomozygous117149182
8116690826116690827GT48GENICpossibly homozygous116669931
8116690942116690943TC38GENIChomozygous117149184
8116690968116690969AG32GENIChomozygous117149185
8116690970116690971AG32GENIChomozygous117149186
8116691400116691401CG36GENIChomozygous117149187
8116692292116692293TG45GENIChomozygous117149188
8116693665116693666TC41GENIChomozygous117149189
8116693668116693669GA42GENIChomozygous117149190
8116694075116694075CA52GENIChomozygous128635194
8116689660116689663TCT22GENICpossibly homozygous128635192
8116690882116690882TGTTGT37GENIChomozygous128635193
8116689857116689858TC51GENICpossibly homozygous116886639
8116696917116696918TC62GENIChomozygous117149191
8116699218116699219AG60GENIChomozygous116669937
8116699286116699287CT53GENIChomozygous117149192
8116699482116699483CT59GENIChomozygous117149193
8116695805116695921TGAACTACTTGCTAAGGCTGGGGATTTAGCTTAGTGGTAGAGCACTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCTGAAAAAAAAAAAAAAAAAAACCATTCCTC21GENICpossibly homozygous131054199