| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:112737771-112738189 | Rare:94; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:112976544-112976928 | Common:3; Rare:188 | ||||
| chr5:113294580-113294675 | Rare:34 | ||||
| chr5:113513633-113513711 | Rare:23 | ||||
| chr5:115169773-115170232 | Rare:161 | ||||
| chr5:115262837-115262930 | Rare:45 | ||||
| chr5:115296512-115296910 | Common:3; Rare:61 | ||||
| chr5:115544619-115544996 | Common:3; Rare:135 | ||||
| chr5:115816482-115816645 | Common:1; Rare:41 | ||||
| chr5:115816649-115816717 | Rare:17 | ||||
| chr5:115841524-115842103 | Common:7; Rare:241 | ||||
| chr5:116084763-116085067 | Common:8; Rare:111 | ||||
| chr5:116085425-116085462 | Rare:5 | ||||
| chr5:116573869-116573991 | Common:1; Rare:39 | ||||
| chr5:119070840-119071182 | Common:4; Rare:105 |