| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:103415089-103415449 | Common:6; Rare:185 | ||||
| chr8:106657553-106657887 | Common:4; Rare:94 | ||||
| chr8:108248638-108248879 | Rare:97 | ||||
| chr8:109334058-109334405 | Common:1; Rare:88 | ||||
| chr8:116755669-116755944 | Common:1; Rare:134 | ||||
| chr8:117520572-117520759 | Common:4; Rare:37 | ||||
| chr8:119832815-119832907 | Common:1; Rare:37 | ||||
| chr8:120445100-120445397 | Common:1; Rare:69 | ||||
| chr8:120811070-120811233 | Common:3; Rare:51 | ||||
| chr8:122781547-122781771 | Common:3; Rare:29 | ||||
| chr8:123396406-123396558 | Common:1; Rare:54 | ||||
| chr8:124474186-124474284 | Common:1; Rare:20 | ||||
| chr8:124474997-124475235 | Rare:91 | ||||
| chr8:124539032-124539280 | Common:2; Rare:123; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124557812-124558060 | Common:4; Rare:79 |