| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179550528-179550572 | Common:2; Rare:10 | ||||
| chr5:179559546-179559805 | Common:1; Rare:74 | ||||
| chr5:179623385-179623499 | Rare:43 | ||||
| chr5:179623593-179623796 | Common:1; Rare:87 | ||||
| chr5:179698575-179699099 | Common:4; Rare:186 | ||||
| chr5:179820702-179820918 | Common:6; Rare:74; Clinvar (benign):2 | ||||
| chr5:179858792-179859047 | Rare:136 | ||||
| chr5:179907828-179908021 | Common:2; Rare:99 | ||||
| chr5:180291919-180292184 | Common:2; Rare:96 | ||||
| chr5:180802766-180802912 | Common:3; Rare:59 | ||||
| chr5:180803834-180803898 | Common:1; Rare:14 | ||||
| chr5:180810083-180810223 | Common:1; Rare:34 | ||||
| chr5:180861121-180861421 | Common:2; Rare:120 | ||||
| chr5:181040011-181040028 | Rare:3 | ||||
| chr5:181040068-181040319 | Rare:52 |