| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111661429-111661664 | Common:3; Rare:63 | ||||
| chr9:111896649-111896804 | Common:3; Rare:60 | ||||
| chr9:112332994-112333091 | Rare:32 | ||||
| chr9:112333473-112333777 | Rare:88 | ||||
| chr9:112379770-112380179 | Common:4; Rare:152 | ||||
| chr9:112890774-112890968 | Common:4; Rare:54 | ||||
| chr9:113056657-113056899 | Common:1; Rare:80; Clinvar:1 | ||||
| chr9:113187990-113188196 | Common:2; Rare:28 | ||||
| chr9:113221235-113221640 | Common:1; Rare:129 | ||||
| chr9:113275371-113275734 | Common:5; Rare:114; Clinvar (pathogenic):1 | ||||
| chr9:113340252-113340372 | Common:2; Rare:29 | ||||
| chr9:113410281-113410705 | Common:3; Rare:125 | ||||
| chr9:113565396-113565581 | Common:1; Rare:35 | ||||
| chr9:114387983-114388166 | Common:1; Rare:52 | ||||
| chr9:114505460-114505554 | Common:1; Rare:38 |