| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139273969-139274135 | Rare:78 | ||||
| chr5:139439453-139439646 | Common:2; Rare:52 | ||||
| chr5:139561100-139561363 | Common:1; Rare:103 | ||||
| chr5:139561728-139561794 | Rare:29 | ||||
| chr5:140564318-140564509 | Common:1; Rare:51 | ||||
| chr5:140564675-140564849 | Rare:52 | ||||
| chr5:140647576-140647924 | Common:5; Rare:143; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691317-140691655 | Common:1; Rare:120; Clinvar:10; Clinvar (benign):1 | ||||
| chr5:141320742-141320928 | Common:2; Rare:64 | ||||
| chr5:141636809-141636957 | Common:2; Rare:69 | ||||
| chr5:141682191-141682328 | Common:1; Rare:45 | ||||
| chr5:141958172-141958425 | Rare:61 | ||||
| chr5:142324979-142325208 | Rare:81 | ||||
| chr5:143404420-143404604 | Common:2; Rare:43 | ||||
| chr5:144170575-144170805 | Common:1; Rare:80 |