| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:119832761-119832877 | Common:2; Rare:47 | ||||
| chr8:119873564-119873868 | Common:3; Rare:89 | ||||
| chr8:120445090-120445465 | Common:1; Rare:98 | ||||
| chr8:120812445-120812588 | Rare:27 | ||||
| chr8:122781599-122781919 | Common:3; Rare:62 | ||||
| chr8:123396365-123396556 | Common:2; Rare:86 | ||||
| chr8:123416367-123416805 | Rare:115 | ||||
| chr8:123768358-123768666 | Common:5; Rare:94 | ||||
| chr8:124474521-124474772 | Common:1; Rare:92 | ||||
| chr8:124474963-124475121 | Rare:54 | ||||
| chr8:124538981-124539287 | Common:2; Rare:157; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091687-125091914 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:126558329-126558628 | Common:1; Rare:111 | ||||
| chr8:127735864-127736076 | Rare:45 | ||||
| chr8:127736134-127736269 | Common:3; Rare:29 |