| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:103372151-103372567 | Common:1; Rare:77 | ||||
| chr8:103414710-103414997 | Rare:117 | ||||
| chr8:103414999-103415490 | Common:6; Rare:247 | ||||
| chr8:104588876-104588906 | Rare:8 | ||||
| chr8:105319123-105319387 | Rare:67 | ||||
| chr8:105319447-105319481 | Rare:6 | ||||
| chr8:105319715-105319913 | Common:1; Rare:43 | ||||
| chr8:106269977-106270207 | Rare:81 | ||||
| chr8:106657553-106657898 | Common:4; Rare:98 | ||||
| chr8:107497267-107497639 | Common:2; Rare:111 | ||||
| chr8:108248604-108248874 | Rare:100 | ||||
| chr8:108443493-108443685 | Common:2; Rare:91 | ||||
| chr8:109333997-109334513 | Common:1; Rare:153 | ||||
| chr8:116755657-116755957 | Common:1; Rare:138 | ||||
| chr8:116874612-116874929 | Common:6; Rare:134; Clinvar (benign):1 |