| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:57173581-57173875 | Common:2; Rare:101 | ||||
| chr5:58459762-58460246 | Common:7; Rare:188 | ||||
| chr5:59768012-59768110 | Rare:17 | ||||
| chr5:59768632-59768723 | Rare:27 | ||||
| chr5:59768802-59768893 | Rare:15 | ||||
| chr5:60488061-60488328 | Rare:45 | ||||
| chr5:60522111-60522286 | Common:2; Rare:32 | ||||
| chr5:60700084-60700224 | Common:1; Rare:56 | ||||
| chr5:60844151-60844459 | Common:5; Rare:99 | ||||
| chr5:60945026-60945245 | Common:5; Rare:84; Clinvar:3; Clinvar (benign):5 | ||||
| chr5:61162395-61162644 | Common:1; Rare:72 | ||||
| chr5:62306134-62306481 | Common:3; Rare:129; Clinvar (benign):2 | ||||
| chr5:62403821-62403950 | Common:1; Rare:55 | ||||
| chr5:64768423-64768464 | Common:1; Rare:12 | ||||
| chr5:64768513-64768541 | Rare:9 |