| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112333526-112333941 | Rare:126 | ||||
| chr9:112379759-112380259 | Common:4; Rare:179 | ||||
| chr9:113221230-113221645 | Common:1; Rare:130 | ||||
| chr9:113275348-113275746 | Common:5; Rare:130; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340431 | Common:3; Rare:49 | ||||
| chr9:113376879-113377161 | Common:9; Rare:87 | ||||
| chr9:113397215-113397510 | Common:1; Rare:38 | ||||
| chr9:113410274-113410736 | Common:3; Rare:141 | ||||
| chr9:113463600-113463769 | Common:1; Rare:57 | ||||
| chr9:114077492-114077789 | Common:1; Rare:53 | ||||
| chr9:114098428-114098533 | Common:5; Rare:23 | ||||
| chr9:114323657-114324093 | Common:5; Rare:160 | ||||
| chr9:114387983-114388119 | Common:1; Rare:45 | ||||
| chr9:114587554-114587908 | Common:3; Rare:141 | ||||
| chr9:116687203-116687355 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):1 |