chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73661102236611023GA18GENIChomozygous131032457
73661136636611367TC15GENIChomozygous115646943
73661191036611911AG10GENIChomozygous115646944
73661486636614867TC16GENIChomozygous115646950
73661242436612425T15GENIChomozygous131011805
73661408336614084G6GENIChomozygous131011806
73661781336617814TC8GENIChomozygous131032458
73661238036612380C8GENIChomozygous128453213
73661946136619462TC16GENIChomozygous115646957
73662021136620212CG9GENIChomozygous115646958
73662064036620641GA9GENIChomozygous115646959
73662236036622361GC13GENIChomozygous115646961
73662742636627434TGAGTGAA14GENIChomozygous131011807
73662757536627576GC15GENIChomozygous115646968
73662841736628417C10GENIChomozygous128453221
73662846736628471ATTT14GENIChomozygous128453222
73662877336628774AG22GENIChomozygous118347000
73662933536629336GA19GENIChomozygous118347001
73663029036630403AGTGAAAACTATTCTTTTTTTTTTTTTTTTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC11GENIChomozygous128453227
73663174636631746GG2GENIChomozygous131011808
73663174836631748C2GENIChomozygous131011809
73663175636631761GGTTC2GENIChomozygous131011810
73663182636631827TC7GENIChomozygous115646977
73663196636631967AG10GENIChomozygous115646978
73663372136633721ATC6GENIChomozygous128453228
73663383236633833TC17GENIChomozygous115646979
73663388436633885TC16GENIChomozygous118347003
73663449236634493AT17GENIChomozygous118347004
73663513436635135TC21GENIChomozygous115646981
73663520336635222CACTACACACTACACATCC20GENIChomozygous128453230
73663525436635254AA16GENIChomozygous128453231
73663529136635292GA14GENIChomozygous131032459
73663603236636033AG11GENIChomozygous118347006
73663871036638711CG13GENIChomozygous131032460
73663931536639316AT16GENIChomozygous118347009
73661872336618724AG11GENIChomozygous126568648
73662031936620320AG9GENIChomozygous126568649
73662441536624416GA17GENIChomozygous126568650