| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:80472514-80472855 | Common:2; Rare:58 | ||||
| chr5:81259761-81259946 | Common:1; Rare:54 | ||||
| chr5:83059816-83060060 | Common:2; Rare:44 | ||||
| chr5:87331108-87331436 | Common:1; Rare:79; Clinvar (benign):3 | ||||
| chr5:87340293-87340991 | Common:1; Rare:120 | ||||
| chr5:87348658-87348902 | Common:1; Rare:44 | ||||
| chr5:87355090-87355338 | Rare:45 | ||||
| chr5:87366719-87366940 | Rare:47 | ||||
| chr5:87368481-87368715 | Rare:42 | ||||
| chr5:87369574-87369874 | Rare:45; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr5:87371524-87371730 | Common:1; Rare:41 | ||||
| chr5:87383825-87383877 | Rare:11 | ||||
| chr5:87383885-87383913 | Rare:3 | ||||
| chr5:87383923-87384007 | Rare:13 | ||||
| chr5:87388372-87388537 | Rare:43 |