| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34929754-34929904 | Rare:59 | ||||
| chr5:36151885-36152168 | Rare:87 | ||||
| chr5:36876642-36876844 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr5:38845715-38846096 | Common:2; Rare:100 | ||||
| chr5:41870361-41870397 | Rare:19; Clinvar:1 | ||||
| chr5:43483837-43483965 | Common:1; Rare:45 | ||||
| chr5:43603072-43603252 | Rare:45 | ||||
| chr5:44808661-44808965 | Common:2; Rare:96 | ||||
| chr5:50667759-50667918 | Common:1; Rare:51 | ||||
| chr5:53109739-53109877 | Common:1; Rare:66; Clinvar:2 | ||||
| chr5:55307639-55308010 | Common:4; Rare:122 | ||||
| chr5:55994898-55995167 | Rare:92 | ||||
| chr5:60945012-60945240 | Common:5; Rare:91; Clinvar:3; Clinvar (benign):5 | ||||
| chr5:61162366-61162624 | Common:1; Rare:72 | ||||
| chr5:62403808-62404032 | Common:3; Rare:83 |