chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154148178154148179TC21GENIChomozygous108316032
1154148417154148418TA32GENIChomozygous108316034
1154150045154150046TA23GENIChomozygous108316036
1154151285154151286GA21GENIChomozygous108316038
1154151719154151720GT32GENIChomozygous108316040
1154153070154153071GA36GENIChomozygous108316042
1154153779154153780TC38GENIChomozygous108316044
1154155137154155138CA41GENIChomozygous108316046
1154155878154155879GA22GENIChomozygous108316048
1154156354154156355GC35GENIChomozygous108316050
1154159100154159101CT16GENIChomozygous108316052
1154159305154159306TC21GENIChomozygous108316054
1154159607154159608AG30GENIChomozygous108316056
1154161570154161571CA24GENIChomozygous108316058
1154163062154163063CG40GENIChomozygous108316060
1154163695154163696GA20GENIChomozygous108316062
1154163729154163730TC16GENIChomozygous108316064
1154165198154165199GA23GENIChomozygous108316066