| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138874907-138875230 | Common:1; Rare:72 | ||||
| chr5:138875233-138875513 | Rare:55; Clinvar (benign):1 | ||||
| chr5:138875597-138875707 | Rare:21 | ||||
| chr5:139198280-139198531 | Rare:83; Clinvar (benign):1 | ||||
| chr5:139273698-139273859 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr5:139273945-139274142 | Rare:90 | ||||
| chr5:139293535-139294018 | Rare:150 | ||||
| chr5:139341662-139341960 | Common:1; Rare:84 | ||||
| chr5:139404056-139404208 | Rare:55 | ||||
| chr5:139439441-139439646 | Common:2; Rare:56 | ||||
| chr5:139561100-139561387 | Common:1; Rare:114 | ||||
| chr5:139561727-139561800 | Rare:31 | ||||
| chr5:139648168-139648374 | Rare:58 | ||||
| chr5:140175017-140175247 | Rare:60 | ||||
| chr5:140303039-140303200 | Common:1; Rare:57 |