chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107868797778687978CG13GENIChomozygous117345226
107868803378688034GA25GENIChomozygous116645012
107868818278688183GA8GENIChomozygous116645014
107868886578688866TA13GENIChomozygous116645016
107869116678691167TC22GENIChomozygous116645018
107869125878691259TC33GENIChomozygous116645020
107869149278691493GC5GENIChomozygous116807178
107869169978691700TG7GENIChomozygous116645022
107869218678692187GA21GENIChomozygous117345230
107869223078692231TC16GENIChomozygous116645024
107869232978692330CG11GENICheterozygous116645026
107869237078692371CT13GENIChomozygous116645028
107869249878692499CT26GENIChomozygous116645030
107869358578693586TG11GENIChomozygous116645032
107869385078693851TC13GENIChomozygous116645034
107869396178693962TC13GENIChomozygous116645036
107869464078694641GA8GENIChomozygous116645038
107869482978694830AG10GENIChomozygous116645040
107869502778695028GA26GENIChomozygous116645042
107869510578695106TC20GENIChomozygous116645044
107869536078695361GT10GENIChomozygous116645046
107869537178695372TC5GENIChomozygous116645048
107869577378695774GT17GENIChomozygous116645050