| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124450206-124450377 | Rare:30 | ||||
| chr8:124450717-124450919 | Common:7; Rare:79 | ||||
| chr8:124474178-124474318 | Common:1; Rare:28 | ||||
| chr8:124474509-124474778 | Common:1; Rare:97 | ||||
| chr8:124474936-124475271 | Rare:117 | ||||
| chr8:124538979-124539287 | Common:2; Rare:159; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124539380-124539496 | Rare:28 | ||||
| chr8:124998210-124998703 | Common:5; Rare:197 | ||||
| chr8:125091626-125091944 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:125430338-125430423 | Common:1; Rare:22 | ||||
| chr8:126557667-126557905 | Rare:56 | ||||
| chr8:126558253-126558638 | Common:2; Rare:130 | ||||
| chr8:127735799-127736470 | Common:4; Rare:160 | ||||
| chr8:129939622-129939888 | Common:1; Rare:98 | ||||
| chr8:130016377-130016453 | Rare:20 |