| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:17216994-17217118 | Common:5; Rare:37 | ||||
| chr5:24644685-24644870 | Common:5; Rare:33 | ||||
| chr5:24644976-24645030 | Rare:8 | ||||
| chr5:31532052-31532352 | Common:3; Rare:87 | ||||
| chr5:32174277-32174389 | Common:1; Rare:42 | ||||
| chr5:33440593-33441079 | Common:6; Rare:129 | ||||
| chr5:34008027-34008214 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34915461-34915752 | Common:1; Rare:75 | ||||
| chr5:35617842-35617928 | Rare:20 | ||||
| chr5:36151871-36152180 | Rare:95 | ||||
| chr5:36606465-36606644 | Rare:30 | ||||
| chr5:36876650-36876894 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371040-37371140 | Rare:40 | ||||
| chr5:38557236-38557308 | Rare:19 | ||||
| chr5:39074346-39074522 | Common:1; Rare:83 |