| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:108443463-108443683 | Common:3; Rare:99 | ||||
| chr8:109334012-109334400 | Common:1; Rare:113 | ||||
| chr8:109539565-109539882 | Common:2; Rare:80 | ||||
| chr8:116766373-116766586 | Common:1; Rare:54 | ||||
| chr8:116874611-116874929 | Common:6; Rare:134; Clinvar (benign):1 | ||||
| chr8:119673340-119673517 | Rare:31 | ||||
| chr8:119832792-119832897 | Common:2; Rare:46 | ||||
| chr8:119855849-119855982 | Common:1; Rare:32 | ||||
| chr8:119873586-119873849 | Common:3; Rare:82 | ||||
| chr8:120445087-120445451 | Common:1; Rare:90 | ||||
| chr8:122781558-122781918 | Common:3; Rare:67 | ||||
| chr8:123396359-123396562 | Common:2; Rare:93 | ||||
| chr8:123506504-123506728 | Common:1; Rare:57 | ||||
| chr8:124474983-124475099 | Rare:38 | ||||
| chr8:124538995-124539186 | Common:2; Rare:112; Clinvar (benign):5 |