chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154148178154148179TC16GENIChomozygous108316032
1154148417154148418TA20GENIChomozygous108316034
1154150045154150046TA14GENIChomozygous108316036
1154151000154151001GA10GENICheterozygous120781426
1154151285154151286GA20GENIChomozygous108316038
1154151719154151720GT22GENIChomozygous108316040
1154153070154153071GA27GENIChomozygous108316042
1154153779154153780TC34GENIChomozygous108316044
1154156354154156355GC24GENIChomozygous108316050
1154159100154159101CT19GENIChomozygous108316052
1154159305154159306TC11GENIChomozygous108316054
1154159607154159608AG25GENIChomozygous108316056
1154161570154161571CA18GENIChomozygous108316058
1154163062154163063CG22GENIChomozygous108316060
1154163695154163696GA23GENIChomozygous108316062
1154163729154163730TC23GENIChomozygous108316064
1154165198154165199GA29GENIChomozygous108316066