| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:108443463-108443674 | Common:3; Rare:94 | ||||
| chr8:109334009-109334412 | Common:1; Rare:117 | ||||
| chr8:109362317-109362544 | Common:1; Rare:44 | ||||
| chr8:109540108-109540216 | Common:1; Rare:17 | ||||
| chr8:109540512-109540642 | Common:1; Rare:29 | ||||
| chr8:109643912-109644128 | Common:2; Rare:43 | ||||
| chr8:109644670-109644853 | Common:1; Rare:59 | ||||
| chr8:115668946-115669254 | Rare:73 | ||||
| chr8:116766372-116766577 | Common:1; Rare:50 | ||||
| chr8:116874150-116874256 | Common:1; Rare:45 | ||||
| chr8:116937984-116938231 | Common:1; Rare:51 | ||||
| chr8:116938425-116938504 | Common:3; Rare:33 | ||||
| chr8:117520541-117520819 | Common:5; Rare:70 | ||||
| chr8:118111266-118111373 | Common:1; Rare:24; Clinvar (benign):2 | ||||
| chr8:118951829-118952149 | Common:1; Rare:91; Clinvar:7; Clinvar (benign):1 |