| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:120445087-120445451 | Common:1; Rare:90 | ||||
| chr8:123072449-123072756 | Common:1; Rare:72 | ||||
| chr8:124474963-124475099 | Rare:44 | ||||
| chr8:124538981-124539204 | Common:2; Rare:127; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:125091710-125091938 | Common:2; Rare:80; Clinvar (benign):3 | ||||
| chr8:126557759-126557907 | Rare:36 | ||||
| chr8:126558389-126558628 | Common:1; Rare:86 | ||||
| chr8:127735870-127736076 | Rare:43 | ||||
| chr8:127736119-127736257 | Common:3; Rare:25 | ||||
| chr8:140511231-140511490 | Common:3; Rare:103 | ||||
| chr8:141001186-141001487 | Common:4; Rare:109 | ||||
| chr8:142669952-142670281 | Common:9; Rare:119 | ||||
| chr8:143018399-143018583 | Common:2; Rare:55 | ||||
| chr8:143334802-143334976 | Common:1; Rare:67 | ||||
| chr8:143541430-143541673 | Common:3; Rare:78 |