chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97697090076970901AG28GENIChomozygous148182095
97697260676972607G15GENIChomozygous143398011
97697400376974004GA15GENIChomozygous143409718
97697598176975982AT30GENICpossibly homozygous143409722
97698127276981273A18GENIChomozygous143398012
97698168476981684TGAATGAA11GENIChomozygous143398014
97698823476988235CT11GENIChomozygous148182100
97697722476977225GT17GENIChomozygous143409723
97697929776979298CT21GENIChomozygous148182096
97698133876981339CT23GENIChomozygous148182097
97698514576985146CT18GENIChomozygous148182098
97698613976986140CT17GENIChomozygous148182099
97698675176986752TC18GENIChomozygous143409734
97698697876986979TC14GENIChomozygous143409735
97698746376987464TC22GENIChomozygous143409736
97698265376982653A28GENIChomozygous148179095
97698928176989295GTAGTAGTAGTAGT8GENIChomozygous148179096
97699083976990840AC24GENIChomozygous143409739
97699147376991474AG21GENIChomozygous143409740
97699178676991787TC23GENIChomozygous143409741
97699231076992311CG26GENIChomozygous143409742
97699281876992819CA25GENIChomozygous148182101
97698928176989282G9GENICpossibly homozygous403936770
97698928176989282GA9GENICheterozygous403936771