| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:109334074-109334402 | Common:1; Rare:83 | ||||
| chr8:116755669-116755923 | Common:1; Rare:125 | ||||
| chr8:116938418-116938471 | Common:1; Rare:16 | ||||
| chr8:117520527-117520753 | Common:5; Rare:50 | ||||
| chr8:119832826-119832923 | Common:1; Rare:35 | ||||
| chr8:119873362-119873888 | Common:3; Rare:135 | ||||
| chr8:120445099-120445420 | Common:1; Rare:75 | ||||
| chr8:120811052-120811231 | Common:3; Rare:61 | ||||
| chr8:122781589-122781769 | Common:3; Rare:25 | ||||
| chr8:123274237-123274321 | Rare:8 | ||||
| chr8:123396186-123396492 | Common:1; Rare:152 | ||||
| chr8:124474186-124474333 | Common:1; Rare:31 | ||||
| chr8:124474562-124474781 | Rare:79 | ||||
| chr8:124474966-124475119 | Rare:53 | ||||
| chr8:124538992-124539280 | Common:2; Rare:149; Clinvar (benign):7; Clinvar (pathogenic):1 |