| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:118951863-118951928 | Rare:21; Clinvar:1 | ||||
| chr8:118951960-118952173 | Common:1; Rare:59; Clinvar:6; Clinvar (benign):1 | ||||
| chr8:119832815-119832894 | Common:1; Rare:31 | ||||
| chr8:120445099-120445404 | Common:1; Rare:70 | ||||
| chr8:123274258-123274321 | Rare:4 | ||||
| chr8:123396393-123396495 | Common:1; Rare:57 | ||||
| chr8:124474535-124474781 | Rare:90 | ||||
| chr8:124538991-124539275 | Common:2; Rare:148; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124998539-124998965 | Common:8; Rare:135 | ||||
| chr8:125091731-125091876 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr8:129939749-129939856 | Rare:39 | ||||
| chr8:133571849-133572273 | Rare:112 | ||||
| chr8:140511287-140511490 | Common:1; Rare:84 | ||||
| chr8:142727006-142727270 | Common:3; Rare:103 | ||||
| chr8:143018383-143018554 | Common:1; Rare:54 |