chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154148178154148179TC8GENIChomozygous108316032
1154148417154148418TA17GENIChomozygous108316034
1154150045154150046TA8GENIChomozygous108316036
1154151285154151286GA6GENIChomozygous108316038
1154151719154151720GT18GENIChomozygous108316040
1154153070154153071GA6GENIChomozygous108316042
1154153779154153780TC20GENIChomozygous108316044
1154155137154155138CA16GENIChomozygous108316046
1154156354154156355GC21GENIChomozygous108316050
1154159100154159101CT5GENIChomozygous108316052
1154159305154159306TC5GENIChomozygous108316054
1154159607154159608AG21GENIChomozygous108316056
1154163062154163063CG10GENIChomozygous108316060
1154163695154163696GA12GENIChomozygous108316062
1154163729154163730TC9GENIChomozygous108316064
1154165198154165199GA12GENIChomozygous108316066
1154163144154163145AG6GENICheterozygous125402598