| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:126558346-126558628 | Common:1; Rare:104 | ||||
| chr8:127735866-127736082 | Rare:48 | ||||
| chr8:127736109-127736329 | Common:3; Rare:54 | ||||
| chr8:129939740-129939847 | Rare:40 | ||||
| chr8:130443507-130443686 | Common:4; Rare:53 | ||||
| chr8:131904024-131904215 | Common:1; Rare:77 | ||||
| chr8:132675529-132675670 | Rare:41 | ||||
| chr8:133297163-133297481 | Common:3; Rare:124; Clinvar:4; Clinvar (benign):1 | ||||
| chr8:133570262-133570799 | Common:1; Rare:122 | ||||
| chr8:133571793-133572241 | Common:1; Rare:112 | ||||
| chr8:134713010-134713212 | Common:1; Rare:68 | ||||
| chr8:140511226-140511585 | Common:3; Rare:134 | ||||
| chr8:141001124-141001496 | Common:4; Rare:129 | ||||
| chr8:142669939-142670270 | Common:8; Rare:124 | ||||
| chr8:142777139-142777657 | Common:7; Rare:117 |