| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39697936-39698192 | Common:2; Rare:109 | ||||
| chr4:40056587-40057014 | Common:4; Rare:127 | ||||
| chr4:40629462-40629877 | Rare:87 | ||||
| chr4:40629882-40629900 | Rare:3 | ||||
| chr4:40749887-40750223 | Common:2; Rare:91 | ||||
| chr4:41214433-41214730 | Common:5; Rare:77 | ||||
| chr4:41256706-41256994 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:41692747-41692917 | Common:7; Rare:34 | ||||
| chr4:41935055-41935256 | Common:3; Rare:59 | ||||
| chr4:41981678-41981843 | Common:2; Rare:53 | ||||
| chr4:41990379-41990597 | Common:1; Rare:79 | ||||
| chr4:42152641-42152735 | Rare:28 | ||||
| chr4:42656943-42657240 | Common:7; Rare:103 | ||||
| chr4:42657422-42657520 | Rare:22 | ||||
| chr4:44678387-44678750 | Common:1; Rare:137 |