| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138178604-138178873 | Rare:52 | ||||
| chr5:138178935-138179178 | Common:3; Rare:51 | ||||
| chr5:138331753-138332122 | Common:2; Rare:94 | ||||
| chr5:138543074-138543569 | Common:2; Rare:159 | ||||
| chr5:138753261-138753503 | Common:2; Rare:85 | ||||
| chr5:139198277-139198538 | Rare:88; Clinvar (benign):1 | ||||
| chr5:139273978-139274135 | Rare:74 | ||||
| chr5:139383273-139383460 | Rare:36 | ||||
| chr5:139388374-139388491 | Common:2; Rare:23 | ||||
| chr5:139561112-139561409 | Common:1; Rare:118 | ||||
| chr5:139561733-139561811 | Rare:29 | ||||
| chr5:139648186-139648392 | Common:1; Rare:61 | ||||
| chr5:140108014-140108172 | Rare:50 | ||||
| chr5:140174932-140175280 | Common:1; Rare:101 | ||||
| chr5:140303065-140303165 | Common:1; Rare:29 |