| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:141102154-141102323 | Common:2; Rare:75 | ||||
| chr5:141172547-141172664 | Common:1; Rare:25 | ||||
| chr5:141320600-141320939 | Common:3; Rare:103 | ||||
| chr5:141618910-141619256 | Common:1; Rare:111; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:141636803-141637001 | Common:2; Rare:90 | ||||
| chr5:141637235-141637459 | Common:1; Rare:50 | ||||
| chr5:141682195-141682328 | Common:1; Rare:43 | ||||
| chr5:141923721-141923956 | Common:1; Rare:72 | ||||
| chr5:141924077-141924125 | Common:2; Rare:8 | ||||
| chr5:141966758-141966872 | Rare:18 | ||||
| chr5:141968817-141969230 | Common:3; Rare:114 | ||||
| chr5:142012986-142013088 | Rare:32 | ||||
| chr5:142108675-142109034 | Common:4; Rare:116 | ||||
| chr5:142324936-142325194 | Rare:100 | ||||
| chr5:142770171-142770435 | Rare:92 |