| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123416398-123416846 | Common:1; Rare:113 | ||||
| chr8:123540995-123541380 | Common:3; Rare:129 | ||||
| chr8:124372675-124372857 | Common:1; Rare:62 | ||||
| chr8:124474526-124474714 | Rare:73 | ||||
| chr8:124474946-124475165 | Rare:74 | ||||
| chr8:124539026-124539287 | Common:2; Rare:128; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124546845-124547089 | Rare:54; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:125091710-125091914 | Common:2; Rare:71; Clinvar (benign):3 | ||||
| chr8:126558346-126558638 | Common:1; Rare:109 | ||||
| chr8:127735872-127736086 | Rare:46 | ||||
| chr8:127736118-127736277 | Common:3; Rare:33 | ||||
| chr8:132675529-132675653 | Rare:35 | ||||
| chr8:133297185-133297500 | Common:3; Rare:125; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:133571810-133572168 | Rare:87 | ||||
| chr8:134713017-134713175 | Common:1; Rare:52 |