| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34915445-34915789 | Common:1; Rare:97 | ||||
| chr5:35617687-35617928 | Common:1; Rare:49 | ||||
| chr5:36066853-36067007 | Rare:35 | ||||
| chr5:36151794-36152233 | Rare:122 | ||||
| chr5:36242126-36242334 | Common:1; Rare:57 | ||||
| chr5:36606465-36606642 | Rare:30 | ||||
| chr5:36876616-36876889 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37249266-37249593 | Common:1; Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37370961-37371382 | Common:2; Rare:120 | ||||
| chr5:37379034-37379375 | Common:3; Rare:79 | ||||
| chr5:39074373-39074539 | Common:1; Rare:76 | ||||
| chr5:40755839-40756130 | Common:1; Rare:76 | ||||
| chr5:40798152-40798500 | Common:2; Rare:138 | ||||
| chr5:40835117-40835418 | Common:2; Rare:128 | ||||
| chr5:40835650-40835673 | Rare:6 |