| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:40679708-40679929 | Common:1; Rare:46 | ||||
| chr5:40755848-40756127 | Common:1; Rare:74 | ||||
| chr5:40798089-40798448 | Common:1; Rare:136 | ||||
| chr5:40834985-40835433 | Common:3; Rare:173 | ||||
| chr5:40835622-40835658 | Rare:9 | ||||
| chr5:40841281-40841385 | Rare:24 | ||||
| chr5:40841541-40841651 | Common:1; Rare:33 | ||||
| chr5:41870341-41870606 | Common:2; Rare:89; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:41903993-41904383 | Common:2; Rare:120 | ||||
| chr5:43064815-43065144 | Common:1; Rare:78 | ||||
| chr5:43067127-43067495 | Rare:61 | ||||
| chr5:43067582-43067609 | Rare:5 | ||||
| chr5:43120838-43120968 | Common:3; Rare:63 | ||||
| chr5:43121404-43121684 | Common:1; Rare:105 | ||||
| chr5:43121932-43122044 | Common:1; Rare:45 |