| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179820763-179820934 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179858763-179859050 | Rare:153 | ||||
| chr5:179907760-179908130 | Common:5; Rare:152 | ||||
| chr5:180071698-180071841 | Common:1; Rare:63 | ||||
| chr5:180072085-180072245 | Common:2; Rare:65 | ||||
| chr5:180292020-180292259 | Common:1; Rare:90 | ||||
| chr5:180352203-180352849 | Common:3; Rare:278 | ||||
| chr5:180353329-180353514 | Common:4; Rare:73 | ||||
| chr5:180494153-180494427 | Common:2; Rare:90 | ||||
| chr5:180494891-180495059 | Common:2; Rare:58 | ||||
| chr5:180618657-180618826 | Common:3; Rare:70; Clinvar (benign):1 | ||||
| chr5:180809801-180809951 | Common:4; Rare:29 | ||||
| chr5:180810010-180810350 | Common:7; Rare:97 | ||||
| chr5:180810370-180810730 | Common:12; Rare:131 | ||||
| chr5:180810734-180811244 | Common:10; Rare:180 |