| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:78648729-78648981 | Common:2; Rare:88 | ||||
| chr5:79069618-79069777 | Rare:54; Clinvar (benign):2 | ||||
| chr5:79512795-79512889 | Rare:20 | ||||
| chr5:79513094-79513286 | Common:1; Rare:38 | ||||
| chr5:79514527-79514708 | Rare:54 | ||||
| chr5:79612237-79612556 | Rare:81 | ||||
| chr5:79689720-79690056 | Common:3; Rare:99 | ||||
| chr5:79991175-79991354 | Rare:57 | ||||
| chr5:80256028-80256270 | Common:1; Rare:96 | ||||
| chr5:80407856-80408108 | Common:1; Rare:93 | ||||
| chr5:80488007-80488145 | Common:1; Rare:53 | ||||
| chr5:80654539-80654720 | Common:5; Rare:108 | ||||
| chr5:81233149-81233377 | Common:1; Rare:57 | ||||
| chr5:81301470-81301698 | Common:5; Rare:79 | ||||
| chr5:81750990-81751469 | Common:1; Rare:144 |