| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:119638818-119639031 | Common:1; Rare:31 | ||||
| chr8:119832746-119832929 | Common:2; Rare:70 | ||||
| chr8:119855864-119855975 | Common:1; Rare:26 | ||||
| chr8:119873564-119873883 | Common:3; Rare:94 | ||||
| chr8:120445085-120445440 | Common:1; Rare:87 | ||||
| chr8:121641400-121641562 | Rare:27 | ||||
| chr8:122781589-122781926 | Common:3; Rare:65 | ||||
| chr8:123042191-123042583 | Common:3; Rare:96 | ||||
| chr8:123274409-123274711 | Common:2; Rare:98 | ||||
| chr8:123396359-123396519 | Common:1; Rare:80 | ||||
| chr8:124372457-124372553 | Rare:26 | ||||
| chr8:124450859-124450889 | Rare:11 | ||||
| chr8:124474555-124474778 | Rare:79 | ||||
| chr8:124474949-124475123 | Rare:57 | ||||
| chr8:124539042-124539251 | Common:2; Rare:105; Clinvar (benign):7; Clinvar (pathogenic):1 |