| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:126557712-126557915 | Rare:49 | ||||
| chr8:126558273-126558628 | Common:1; Rare:123 | ||||
| chr8:127735866-127736086 | Rare:49 | ||||
| chr8:127736119-127736334 | Common:3; Rare:53 | ||||
| chr8:129752861-129753189 | Common:1; Rare:73 | ||||
| chr8:129939708-129939855 | Rare:53 | ||||
| chr8:132675507-132675665 | Rare:51 | ||||
| chr8:132775227-132775608 | Common:2; Rare:138 | ||||
| chr8:132866698-132867283 | Common:4; Rare:139; Clinvar:1 | ||||
| chr8:132881849-132882712 | Common:2; Rare:189; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr8:132898154-132898396 | Common:3; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:132919025-132919638 | Common:2; Rare:139; Clinvar:2; Clinvar (benign):2 | ||||
| chr8:132964058-132964565 | Common:3; Rare:101 | ||||
| chr8:132968609-132968964 | Common:5; Rare:58 | ||||
| chr8:132969327-132969671 | Common:3; Rare:106; Clinvar:2; Clinvar (benign):1 |