| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:122781588-122781758 | Common:3; Rare:24 | ||||
| chr8:124474877-124475099 | Common:1; Rare:70 | ||||
| chr8:124539042-124539188 | Common:2; Rare:82; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124998270-124998640 | Common:4; Rare:152 | ||||
| chr8:125091709-125091909 | Common:2; Rare:70; Clinvar (benign):3 | ||||
| chr8:127735890-127736083 | Rare:44 | ||||
| chr8:127736118-127736294 | Common:3; Rare:38 | ||||
| chr8:129939753-129939863 | Rare:40 | ||||
| chr8:133571854-133572185 | Rare:81 | ||||
| chr8:141001142-141001407 | Common:2; Rare:85 | ||||
| chr8:143018438-143018558 | Common:1; Rare:35 | ||||
| chr8:143541424-143541658 | Common:2; Rare:78 | ||||
| chr8:143558262-143558390 | Common:1; Rare:48 | ||||
| chr8:143617452-143617753 | Common:2; Rare:111 | ||||
| chr8:143635893-143636051 | Common:2; Rare:67 |