| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:22109345-22109613 | Common:14; Rare:218 | ||||
| chr8:22164760-22165430 | Common:12; Rare:260; Clinvar:2; Clinvar (benign):7 | ||||
| chr8:22245019-22245455 | Common:4; Rare:313 | ||||
| chr8:22367002-22367836 | Common:11; Rare:390 | ||||
| chr8:22404390-22404990 | Common:27; Rare:287 | ||||
| chr8:22440880-22441267 | Common:13; Rare:194 | ||||
| chr8:22551047-22551447 | Common:6; Rare:118 | ||||
| chr8:22551520-22551938 | Common:2; Rare:138 | ||||
| chr8:22554152-22554269 | Common:1; Rare:27 | ||||
| chr8:22556444-22556810 | Common:3; Rare:123 | ||||
| chr8:22588660-22589040 | Common:5; Rare:106 | ||||
| chr8:22589067-22589344 | Common:8; Rare:188 | ||||
| chr8:22604527-22604862 | Common:4; Rare:237 | ||||
| chr8:22604986-22605088 | Common:1; Rare:29 | ||||
| chr8:22669070-22669199 | Common:4; Rare:76 |