| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:102412697-102412948 | Common:3; Rare:62 | ||||
| chr8:102864146-102864324 | Rare:80 | ||||
| chr8:103298702-103298935 | Common:1; Rare:58 | ||||
| chr8:103415050-103415458 | Common:6; Rare:214 | ||||
| chr8:106657548-106657928 | Common:5; Rare:110 | ||||
| chr8:108248638-108248879 | Rare:97 | ||||
| chr8:108443437-108443661 | Common:4; Rare:97 | ||||
| chr8:109334029-109334402 | Common:1; Rare:107 | ||||
| chr8:109539463-109539910 | Common:3; Rare:111 | ||||
| chr8:115667970-115668052 | Rare:11 | ||||
| chr8:115668946-115669306 | Rare:85 | ||||
| chr8:116755783-116755875 | Rare:53 | ||||
| chr8:116766321-116766586 | Common:4; Rare:69 | ||||
| chr8:116874611-116874976 | Common:6; Rare:155; Clinvar (benign):1 | ||||
| chr8:116938397-116938519 | Common:4; Rare:50 |