| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:31193484-31193814 | Common:4; Rare:70 | ||||
| chr5:31532043-31532372 | Common:3; Rare:96 | ||||
| chr5:32174277-32174389 | Common:1; Rare:42 | ||||
| chr5:33440611-33441083 | Common:6; Rare:125 | ||||
| chr5:34008027-34008222 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34915453-34915744 | Common:1; Rare:72 | ||||
| chr5:36151838-36152153 | Rare:82 | ||||
| chr5:36606373-36606631 | Rare:44; Clinvar (benign):1 | ||||
| chr5:36876639-36876885 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371042-37371338 | Common:1; Rare:75 | ||||
| chr5:38557246-38557502 | Rare:64 | ||||
| chr5:39074381-39074522 | Common:1; Rare:64 | ||||
| chr5:40755884-40756017 | Rare:36 | ||||
| chr5:40798152-40798448 | Common:1; Rare:116 | ||||
| chr5:40835181-40835467 | Common:3; Rare:110 |