| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140647486-140647919 | Common:5; Rare:180; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:140691251-140691748 | Common:2; Rare:185; Clinvar:13; Clinvar (benign):3 | ||||
| chr5:141223523-141223790 | Common:1; Rare:93 | ||||
| chr5:141320306-141320429 | Rare:34 | ||||
| chr5:141320633-141320933 | Common:3; Rare:92 | ||||
| chr5:141417920-141418069 | Common:1; Rare:54 | ||||
| chr5:141524753-141525028 | Common:2; Rare:53 | ||||
| chr5:141634717-141634904 | Rare:34 | ||||
| chr5:141636805-141637017 | Common:2; Rare:92 | ||||
| chr5:141637353-141637681 | Common:1; Rare:71 | ||||
| chr5:141682179-141682328 | Common:1; Rare:47 | ||||
| chr5:141923756-141923909 | Common:1; Rare:42 | ||||
| chr5:141923961-141924214 | Common:3; Rare:62 | ||||
| chr5:142108931-142109032 | Common:1; Rare:30 | ||||
| chr5:142324911-142325248 | Rare:122 |