| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140647585-140647923 | Common:5; Rare:138; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691313-140691661 | Common:1; Rare:124; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:141320742-141320912 | Common:1; Rare:58 | ||||
| chr5:141636803-141637011 | Common:2; Rare:93 | ||||
| chr5:141680816-141681140 | Common:1; Rare:65 | ||||
| chr5:141682191-141682328 | Common:1; Rare:45 | ||||
| chr5:141968989-141969248 | Common:3; Rare:80 | ||||
| chr5:142324979-142325300 | Rare:105 | ||||
| chr5:143404426-143404569 | Common:2; Rare:36 | ||||
| chr5:146182500-146182875 | Common:4; Rare:111 | ||||
| chr5:147509889-147510140 | Rare:61 | ||||
| chr5:148383858-148384026 | Rare:53 | ||||
| chr5:149271679-149271958 | Common:3; Rare:95 | ||||
| chr5:149345355-149345657 | Common:2; Rare:117 | ||||
| chr5:149551344-149551625 | Rare:67 |