| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184733994-184734403 | Common:8; Rare:169 | ||||
| chr4:184812219-184812410 | Rare:31 | ||||
| chr4:184825927-184826246 | Common:7; Rare:105 | ||||
| chr4:184826751-184826914 | Common:1; Rare:31 | ||||
| chr4:185143145-185143447 | Common:3; Rare:97; Clinvar:1; Clinvar (benign):6 | ||||
| chr4:185182473-185182596 | Rare:17 | ||||
| chr4:185203802-185204162 | Common:7; Rare:107 | ||||
| chr4:185378810-185379107 | Common:4; Rare:57 | ||||
| chr4:185396489-185396719 | Rare:82 | ||||
| chr4:185425864-185426328 | Common:4; Rare:150 | ||||
| chr4:185470958-185471412 | Common:10; Rare:79 | ||||
| chr4:185471674-185471810 | Common:1; Rare:57 | ||||
| chr4:185535352-185535640 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:186104571-186104689 | Common:2; Rare:37 | ||||
| chr4:186191451-186191850 | Common:7; Rare:129; Clinvar:3; Clinvar (benign):5 |