| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111599623-111599940 | Common:2; Rare:85 | ||||
| chr9:111631137-111631369 | Common:1; Rare:64 | ||||
| chr9:111661484-111661698 | Common:3; Rare:59 | ||||
| chr9:112333582-112333941 | Rare:113 | ||||
| chr9:112379794-112380146 | Common:4; Rare:141 | ||||
| chr9:113056674-113056883 | Rare:72 | ||||
| chr9:113221230-113221640 | Common:1; Rare:130 | ||||
| chr9:113275359-113275759 | Common:5; Rare:131; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340428 | Common:3; Rare:48 | ||||
| chr9:113410226-113410747 | Common:4; Rare:160 | ||||
| chr9:113564871-113565073 | Common:1; Rare:44 | ||||
| chr9:114587420-114587901 | Common:4; Rare:165 | ||||
| chr9:115118061-115118118 | Common:2; Rare:14 | ||||
| chr9:115118144-115118403 | Rare:65 | ||||
| chr9:116153565-116153910 | Common:1; Rare:82 |