| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124474562-124474769 | Rare:74 | ||||
| chr8:124475001-124475112 | Rare:39 | ||||
| chr8:124538981-124539287 | Common:2; Rare:157; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091626-125091938 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:126558307-126558628 | Common:1; Rare:117 | ||||
| chr8:127735862-127736353 | Common:3; Rare:117 | ||||
| chr8:131904298-131904322 | Rare:5 | ||||
| chr8:132675536-132675702 | Rare:50 | ||||
| chr8:133254577-133254769 | Common:1; Rare:44; Clinvar (pathogenic):1 | ||||
| chr8:133297194-133297481 | Common:3; Rare:118; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:133489633-133490032 | Common:5; Rare:71 | ||||
| chr8:133570313-133570467 | Rare:38 | ||||
| chr8:133571817-133572201 | Rare:94 | ||||
| chr8:134713020-134713230 | Common:1; Rare:75 | ||||
| chr8:140511257-140511633 | Common:2; Rare:141 |