chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154148178154148179TC30GENIChomozygous108316032
1154148417154148418TA76GENIChomozygous108316034
1154150045154150046TA82GENICpossibly homozygous108316036
1154151285154151286GA83GENIChomozygous108316038
1154151719154151720GT65GENIChomozygous108316040
1154153070154153071GA53GENIChomozygous108316042
1154153779154153780TC49GENIChomozygous108316044
1154155137154155138CA56GENIChomozygous108316046
1154155878154155879GA51GENICpossibly homozygous108316048
1154156354154156355GC58GENIChomozygous108316050
1154159100154159101CT76GENIChomozygous108316052
1154159305154159306TC84GENIChomozygous108316054
1154159607154159608AG56GENIChomozygous108316056
1154161570154161571CA50GENIChomozygous108316058
1154163062154163063CG51GENIChomozygous108316060
1154163695154163696GA112GENIChomozygous108316062
1154163729154163730TC97GENIChomozygous108316064
1154165198154165199GA60GENIChomozygous108316066