| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37890992-37891125 | Common:1; Rare:41 | ||||
| chr4:38664211-38664301 | Rare:32 | ||||
| chr4:38867622-38867833 | Common:2; Rare:76 | ||||
| chr4:39182320-39182550 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366319-39366423 | Rare:33 | ||||
| chr4:39458857-39459133 | Common:3; Rare:158; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527337-39527761 | Common:4; Rare:107 | ||||
| chr4:39527950-39528036 | Rare:22 | ||||
| chr4:39638815-39639160 | Common:1; Rare:122 | ||||
| chr4:39697936-39698192 | Common:2; Rare:109 | ||||
| chr4:41216615-41216803 | Common:2; Rare:40 | ||||
| chr4:41990396-41990620 | Common:1; Rare:77 | ||||
| chr4:44678337-44678552 | Common:2; Rare:71 | ||||
| chr4:44678615-44678706 | Rare:43 | ||||
| chr4:44726487-44726642 | Common:2; Rare:54 |