| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140564556-140564849 | Rare:77 | ||||
| chr5:140647579-140647924 | Common:5; Rare:141; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691309-140691651 | Common:1; Rare:121; Clinvar:10; Clinvar (benign):1 | ||||
| chr5:141320762-141320928 | Common:2; Rare:53 | ||||
| chr5:141636818-141637011 | Common:1; Rare:78 | ||||
| chr5:141637353-141637459 | Common:1; Rare:25 | ||||
| chr5:141682195-141682327 | Common:1; Rare:42 | ||||
| chr5:141923736-141923955 | Common:1; Rare:65 | ||||
| chr5:141929727-141930052 | Common:2; Rare:85 | ||||
| chr5:142324079-142324323 | Common:1; Rare:67 | ||||
| chr5:142324973-142325190 | Rare:81 | ||||
| chr5:143404442-143404617 | Common:2; Rare:36 | ||||
| chr5:145937638-145937801 | Rare:42 | ||||
| chr5:146182501-146182904 | Common:4; Rare:123 | ||||
| chr5:148383729-148384021 | Rare:77 |