| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:117520584-117520797 | Common:4; Rare:52 | ||||
| chr8:119832787-119832876 | Common:2; Rare:39 | ||||
| chr8:120445082-120445445 | Common:1; Rare:90 | ||||
| chr8:122781599-122781918 | Common:3; Rare:62 | ||||
| chr8:123273961-123274027 | Common:1; Rare:17 | ||||
| chr8:123274427-123274711 | Common:2; Rare:94 | ||||
| chr8:123396359-123396557 | Common:2; Rare:90 | ||||
| chr8:124474555-124474772 | Rare:76 | ||||
| chr8:124474953-124475121 | Rare:57 | ||||
| chr8:124539037-124539287 | Common:2; Rare:123; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091687-125091914 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:126558340-126558628 | Common:1; Rare:106 | ||||
| chr8:127735864-127736076 | Rare:45 | ||||
| chr8:129939752-129939863 | Rare:41 | ||||
| chr8:132675534-132675656 | Rare:33 |