| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:18084778-18085029 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr8:19602205-19602285 | Common:1; Rare:24 | ||||
| chr8:19682748-19682936 | Common:5; Rare:55 | ||||
| chr8:21913677-21913854 | Rare:49 | ||||
| chr8:21919530-21919783 | Common:2; Rare:101 | ||||
| chr8:22245024-22245452 | Common:2; Rare:153 | ||||
| chr8:22367110-22367382 | Common:5; Rare:100 | ||||
| chr8:22440954-22441301 | Common:7; Rare:88 | ||||
| chr8:22585119-22585399 | Common:1; Rare:88 | ||||
| chr8:22927779-22928068 | Common:4; Rare:61 | ||||
| chr8:23225091-23225118 | Common:1; Rare:8 | ||||
| chr8:23225119-23225223 | Rare:23 | ||||
| chr8:23457613-23457773 | Common:3; Rare:62 | ||||
| chr8:23706696-23706877 | Common:1; Rare:42 | ||||
| chr8:26382928-26383227 | Common:3; Rare:136 |