Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:47095132-47095359 | Rare:46 | ||||
chr19:47095543-47095606 | Rare:11 | ||||
chr19:47108080-47108143 | Rare:16 | ||||
chr19:47730211-47730291 | Rare:11 | ||||
chr19:48966274-48966726 | Rare:151; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr19:49491460-49491985 | Common:3; Rare:152 | ||||
chr19:49689413-49689605 | Rare:45 | ||||
chr19:51015415-51016157 | Common:5; Rare:229 | ||||
chr19:51033883-51034112 | Common:2; Rare:76 | ||||
chr19:51058507-51058819 | Common:2; Rare:81 | ||||
chr19:55230519-55230640 | Common:3; Rare:55 | ||||
chr19:55241011-55241251 | Common:1; Rare:82 | ||||
chr19:55668510-55668761 | Common:1; Rare:56 | ||||
chr19:58398202-58398531 | Common:3; Rare:71 | ||||
chr19:58550606-58550894 | Common:1; Rare:86 |