| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:119208251-119208467 | Common:3; Rare:87 | ||||
| chr8:119209005-119209169 | Common:5; Rare:39 | ||||
| chr8:119832829-119833149 | Common:2; Rare:84 | ||||
| chr8:119855826-119856007 | Common:2; Rare:54 | ||||
| chr8:120445102-120445465 | Common:1; Rare:94 | ||||
| chr8:123396384-123396584 | Common:2; Rare:87 | ||||
| chr8:124474190-124474326 | Common:1; Rare:31 | ||||
| chr8:124474941-124475099 | Rare:48 | ||||
| chr8:124539040-124539224 | Common:2; Rare:100; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091712-125091914 | Common:2; Rare:70; Clinvar (benign):3 | ||||
| chr8:126557712-126557914 | Rare:48 | ||||
| chr8:126558362-126558628 | Common:1; Rare:100 | ||||
| chr8:127735864-127736263 | Common:3; Rare:81 | ||||
| chr8:129939748-129939963 | Common:1; Rare:71 | ||||
| chr8:133571858-133572133 | Rare:67 |