| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179550372-179550572 | Common:4; Rare:58 | ||||
| chr5:179550778-179550858 | Rare:30 | ||||
| chr5:179559534-179559814 | Common:1; Rare:79 | ||||
| chr5:179623596-179623977 | Common:4; Rare:136 | ||||
| chr5:179698568-179699091 | Common:4; Rare:184 | ||||
| chr5:179806275-179806444 | Rare:48 | ||||
| chr5:179806904-179807063 | Common:3; Rare:53 | ||||
| chr5:179820704-179821110 | Common:6; Rare:146; Clinvar:7; Clinvar (benign):2 | ||||
| chr5:179858797-179859026 | Rare:120 | ||||
| chr5:179907811-179908144 | Common:5; Rare:140 | ||||
| chr5:180071605-180071904 | Common:2; Rare:119 | ||||
| chr5:180331025-180331262 | Common:3; Rare:59 | ||||
| chr5:180353211-180353564 | Common:12; Rare:139 | ||||
| chr5:180649571-180649718 | Rare:51 | ||||
| chr5:180802768-180802976 | Common:8; Rare:82 |