| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:117520651-117520797 | Common:3; Rare:41 | ||||
| chr8:119832798-119832872 | Common:1; Rare:34 | ||||
| chr8:119855912-119856053 | Rare:39 | ||||
| chr8:120445097-120445451 | Common:1; Rare:87 | ||||
| chr8:122781599-122781934 | Common:3; Rare:64 | ||||
| chr8:123416323-123416466 | Rare:39 | ||||
| chr8:124372690-124372819 | Common:1; Rare:40 | ||||
| chr8:124474513-124474778 | Common:1; Rare:96 | ||||
| chr8:124474953-124475099 | Rare:47 | ||||
| chr8:124539042-124539189 | Common:2; Rare:82; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124998176-124998544 | Common:1; Rare:142 | ||||
| chr8:125091731-125091909 | Common:2; Rare:61; Clinvar (benign):2 | ||||
| chr8:126558319-126558628 | Common:1; Rare:115 | ||||
| chr8:127735868-127736076 | Rare:44 | ||||
| chr8:132675529-132675686 | Rare:47 |