| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10249874-10250445 | Common:19; Rare:265; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353564-10353905 | Common:4; Rare:133 | ||||
| chr5:10761085-10761434 | Common:13; Rare:114 | ||||
| chr5:14664551-14664962 | Common:5; Rare:162 | ||||
| chr5:16465625-16465913 | Rare:73 | ||||
| chr5:16936227-16936480 | Common:3; Rare:78 | ||||
| chr5:31532037-31532356 | Common:3; Rare:88 | ||||
| chr5:32173865-32174120 | Rare:81 | ||||
| chr5:32174243-32174389 | Common:1; Rare:57 | ||||
| chr5:32444620-32444838 | Rare:83 | ||||
| chr5:32712010-32712108 | Common:1; Rare:21 | ||||
| chr5:32712165-32712403 | Rare:69 | ||||
| chr5:33440602-33441125 | Common:7; Rare:146 | ||||
| chr5:34656159-34656474 | Common:3; Rare:79 | ||||
| chr5:34915215-34915366 | Rare:41 |