| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:76898060-76898350 | Rare:97 | ||||
| chr4:76949559-76949881 | Common:3; Rare:183 | ||||
| chr4:77075140-77075680 | Common:9; Rare:417 | ||||
| chr4:77075762-77076066 | Common:5; Rare:125 | ||||
| chr4:77075970-77076120 | Common:3; Rare:74 | ||||
| chr4:77076250-77076470 | Common:5; Rare:159 | ||||
| chr4:77818979-77819379 | Common:4; Rare:269 | ||||
| chr4:77862635-77862897 | Common:6; Rare:193 | ||||
| chr4:78057242-78057658 | Common:6; Rare:168 | ||||
| chr4:78775730-78776070 | Rare:155 | ||||
| chr4:78776245-78776406 | Common:2; Rare:139 | ||||
| chr4:78939336-78939513 | Common:2; Rare:160 | ||||
| chr4:80073031-80073282 | Common:2; Rare:133; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:82359250-82359660 | Rare:63 | ||||
| chr4:82372920-82373280 | Rare:232 |