| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:4541970-4542143 | Common:1; Rare:72 | ||||
| chr4:5019361-5019556 | Common:2; Rare:72 | ||||
| chr4:6269591-6269910 | Common:2; Rare:115; Clinvar:4 | ||||
| chr4:6640521-6640726 | Common:3; Rare:88 | ||||
| chr4:6987034-6987249 | Common:1; Rare:61 | ||||
| chr4:7068028-7068410 | Common:9; Rare:131 | ||||
| chr4:7939690-7940014 | Common:1; Rare:136 | ||||
| chr4:8440717-8440799 | Rare:30 | ||||
| chr4:15655289-15655676 | Common:2; Rare:165 | ||||
| chr4:15681458-15681869 | Common:3; Rare:142 | ||||
| chr4:16898404-16898463 | Rare:15 | ||||
| chr4:17614551-17614672 | Common:2; Rare:60 | ||||
| chr4:17810696-17811110 | Common:4; Rare:124 | ||||
| chr4:24584473-24584698 | Rare:75 | ||||
| chr4:25160392-25160725 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):1 |