| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:119208233-119208568 | Common:8; Rare:126 | ||||
| chr8:119208977-119209187 | Common:5; Rare:47 | ||||
| chr8:119416172-119416459 | Common:1; Rare:57 | ||||
| chr8:119832807-119832908 | Common:1; Rare:43 | ||||
| chr8:119855820-119855866 | Common:1; Rare:19 | ||||
| chr8:119855868-119855958 | Common:1; Rare:18 | ||||
| chr8:120445087-120445429 | Common:1; Rare:83 | ||||
| chr8:121641423-121641715 | Common:1; Rare:63 | ||||
| chr8:123241327-123241663 | Common:3; Rare:90 | ||||
| chr8:124474163-124474352 | Common:1; Rare:38 | ||||
| chr8:124474969-124475099 | Rare:44 | ||||
| chr8:124539026-124539216 | Common:2; Rare:104; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091717-125091890 | Common:2; Rare:61; Clinvar (benign):3 | ||||
| chr8:126557641-126557911 | Rare:62 | ||||
| chr8:126558346-126558628 | Common:1; Rare:104 |