| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140557404-140557547 | Common:2; Rare:91 | ||||
| chr5:140564573-140564837 | Rare:73 | ||||
| chr5:140647557-140647888 | Common:5; Rare:136; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664638-140664910 | Common:4; Rare:62 | ||||
| chr5:140691300-140691654 | Common:1; Rare:131; Clinvar:12; Clinvar (benign):1 | ||||
| chr5:141320742-141320928 | Common:2; Rare:64 | ||||
| chr5:141430569-141430636 | Rare:13 | ||||
| chr5:141636803-141636997 | Common:2; Rare:89 | ||||
| chr5:141651355-141651542 | Common:1; Rare:60 | ||||
| chr5:141682195-141682395 | Common:2; Rare:55 | ||||
| chr5:141923570-141923881 | Common:1; Rare:79 | ||||
| chr5:141968980-141969234 | Common:3; Rare:77 | ||||
| chr5:142324973-142325310 | Rare:108 | ||||
| chr5:143404442-143404604 | Common:2; Rare:34 | ||||
| chr5:145835244-145835499 | Common:2; Rare:64 |