| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140547510-140547727 | Common:1; Rare:47 | ||||
| chr5:140557410-140557519 | Rare:69 | ||||
| chr5:140564303-140564462 | Common:1; Rare:46 | ||||
| chr5:140564573-140564837 | Rare:73 | ||||
| chr5:140647585-140647924 | Common:5; Rare:139; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691300-140691646 | Common:1; Rare:125; Clinvar:11; Clinvar (benign):1 | ||||
| chr5:141320719-141320912 | Common:2; Rare:67 | ||||
| chr5:141636786-141637011 | Common:2; Rare:106 | ||||
| chr5:141682195-141682328 | Common:1; Rare:43 | ||||
| chr5:141923526-141923933 | Common:1; Rare:113 | ||||
| chr5:141968989-141969248 | Common:3; Rare:80 | ||||
| chr5:142012986-142013122 | Rare:41 | ||||
| chr5:142324979-142325190 | Rare:78 | ||||
| chr5:144170537-144170724 | Common:1; Rare:73 | ||||
| chr5:146182501-146182854 | Common:3; Rare:96 |