| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179819360-179819750 | Common:1; Rare:81 | ||||
| chr5:179820704-179820935 | Common:9; Rare:155; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:179821610-179822160 | Common:15; Rare:254 | ||||
| chr5:179858792-179858994 | Rare:219 | ||||
| chr5:179907774-179908032 | Common:4; Rare:198 | ||||
| chr5:180071677-180071813 | Rare:105 | ||||
| chr5:180072068-180072214 | Common:2; Rare:60 | ||||
| chr5:180291886-180292259 | Common:4; Rare:283 | ||||
| chr5:180494161-180494554 | Common:8; Rare:281 | ||||
| chr5:180494896-180495096 | Common:2; Rare:63 | ||||
| chr5:180802777-180802887 | Common:1; Rare:47 | ||||
| chr5:180810108-180810276 | Common:6; Rare:84 | ||||
| chr5:180810410-180810720 | Common:14; Rare:182 | ||||
| chr5:180860480-180860950 | Common:13; Rare:136 | ||||
| chr5:180861107-180861408 | Common:4; Rare:220 |