| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:90631532-90631565 | Rare:9 | ||||
| chr8:91069222-91069455 | Common:1; Rare:52 | ||||
| chr8:91080468-91080729 | Rare:51; Clinvar (pathogenic):1 | ||||
| chr8:91099749-91100023 | Common:1; Rare:36 | ||||
| chr8:91140119-91140195 | Rare:14 | ||||
| chr8:94640441-94640535 | Rare:18 | ||||
| chr8:94692182-94692404 | Common:1; Rare:46 | ||||
| chr8:94704794-94705055 | Common:1; Rare:39 | ||||
| chr8:94766482-94766678 | Rare:36 | ||||
| chr8:96306317-96306548 | Common:2; Rare:42; Clinvar:1 | ||||
| chr8:97477918-97478181 | Rare:32 | ||||
| chr8:97701460-97701601 | Rare:32 | ||||
| chr8:98136672-98136959 | Rare:73 | ||||
| chr8:98165923-98166132 | Common:2; Rare:35 | ||||
| chr8:98515218-98515229 | Rare:2 |