| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138509137-138509296 | Rare:21 | ||||
| chr5:138933587-138933887 | Common:1; Rare:75 | ||||
| chr5:148111675-148111895 | Common:2; Rare:66; Clinvar (benign):1 | ||||
| chr5:148826278-148826650 | Common:4; Rare:87 | ||||
| chr5:148827669-148827939 | Common:1; Rare:74 | ||||
| chr5:148970422-148970478 | Common:1; Rare:6 | ||||
| chr5:149203269-149203411 | Common:1; Rare:22 | ||||
| chr5:149424681-149424880 | Common:1; Rare:33 | ||||
| chr5:149427914-149427968 | Rare:11 | ||||
| chr5:150404686-150404983 | Common:1; Rare:57 | ||||
| chr5:150778526-150778861 | Common:5; Rare:110 | ||||
| chr5:151566604-151566643 | Rare:9 | ||||
| chr5:159100295-159100705 | Common:4; Rare:124 | ||||
| chr5:172656724-172656940 | Common:1; Rare:35 | ||||
| chr5:172769843-172770322 | Common:2; Rare:119 |