| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179698613-179699111 | Common:4; Rare:174 | ||||
| chr5:179800285-179800591 | Common:1; Rare:92 | ||||
| chr5:179806275-179806485 | Rare:66 | ||||
| chr5:179806839-179807066 | Common:3; Rare:86 | ||||
| chr5:179820851-179820929 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179821075-179821152 | Common:1; Rare:24; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:179822776-179823240 | Common:5; Rare:140; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr5:179823474-179823565 | Common:1; Rare:5 | ||||
| chr5:179823954-179824321 | Common:1; Rare:145; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr5:179907705-179907795 | Rare:21 | ||||
| chr5:180071733-180071813 | Rare:36 | ||||
| chr5:180291851-180292196 | Common:2; Rare:122 | ||||
| chr5:180809813-180810289 | Common:12; Rare:134 | ||||
| chr5:180860548-180860724 | Common:5; Rare:29 | ||||
| chr5:180861198-180861405 | Common:2; Rare:85 |