| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:42992119-42992293 | Common:2; Rare:34 | ||||
| chr5:42993202-42993424 | Common:2; Rare:44 | ||||
| chr5:43041440-43041764 | Common:4; Rare:53 | ||||
| chr5:43041773-43041873 | Rare:23 | ||||
| chr5:43065989-43066054 | Common:1; Rare:8 | ||||
| chr5:43496351-43496489 | Common:1; Rare:28 | ||||
| chr5:55944503-55944618 | Rare:22 | ||||
| chr5:68251905-68252183 | Common:1; Rare:41 | ||||
| chr5:68275137-68275205 | Common:1; Rare:12 | ||||
| chr5:72108230-72108352 | Rare:32 | ||||
| chr5:73087784-73088019 | Rare:48 | ||||
| chr5:77087826-77088228 | Common:3; Rare:77 | ||||
| chr5:78510326-78510500 | Common:1; Rare:41 | ||||
| chr5:80070376-80070694 | Common:1; Rare:72 | ||||
| chr5:87369534-87369847 | Rare:47; Clinvar (benign):1; Clinvar (pathogenic):1 |