| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:157385006-157385062 | Rare:6 | ||||
| chr5:157735932-157735968 | Common:1; Rare:15 | ||||
| chr5:160414328-160414595 | Common:3; Rare:54 | ||||
| chr5:168517768-168517851 | Common:1; Rare:25; Clinvar (benign):2 | ||||
| chr5:169032893-169032967 | Common:5; Rare:10 | ||||
| chr5:169050538-169050740 | Common:1; Rare:33 | ||||
| chr5:169594151-169594678 | Common:3; Rare:172 | ||||
| chr5:169596515-169596626 | Rare:35 | ||||
| chr5:171405232-171405318 | Common:1; Rare:23 | ||||
| chr5:172767116-172767169 | Rare:19 | ||||
| chr5:172769140-172769202 | Rare:16 | ||||
| chr5:172772470-172772623 | Common:3; Rare:32 | ||||
| chr5:176386834-176387020 | Rare:60 | ||||
| chr5:177489943-177490323 | Common:1; Rare:112 | ||||
| chr5:177490946-177491023 | Rare:29 |