| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:113294589-113294679 | Rare:31 | ||||
| chr5:113513624-113513997 | Common:2; Rare:130 | ||||
| chr5:115262808-115262898 | Common:1; Rare:43 | ||||
| chr5:115816532-115816666 | Common:1; Rare:41 | ||||
| chr5:115841461-115842081 | Common:8; Rare:272 | ||||
| chr5:116084687-116085082 | Common:9; Rare:138 | ||||
| chr5:116085370-116085462 | Rare:21 | ||||
| chr5:116495452-116495586 | Common:1; Rare:33 | ||||
| chr5:116574520-116574608 | Common:2; Rare:23 | ||||
| chr5:116574821-116574938 | Common:2; Rare:37 | ||||
| chr5:119070861-119071530 | Common:3; Rare:223 | ||||
| chr5:119268572-119268837 | Common:1; Rare:72 | ||||
| chr5:119333282-119333413 | Common:1; Rare:24 | ||||
| chr5:119355777-119356053 | Common:4; Rare:75 | ||||
| chr5:119452404-119452790 | Common:1; Rare:174; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 |