| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140107683-140107856 | Rare:61 | ||||
| chr5:140174919-140175280 | Common:1; Rare:105 | ||||
| chr5:140303050-140303167 | Common:1; Rare:39 | ||||
| chr5:140346597-140346889 | Common:1; Rare:75 | ||||
| chr5:140547622-140547722 | Common:1; Rare:25 | ||||
| chr5:140564296-140564510 | Common:1; Rare:56 | ||||
| chr5:140564573-140564856 | Rare:77 | ||||
| chr5:140647551-140647924 | Common:5; Rare:156; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:140664750-140664907 | Common:2; Rare:39 | ||||
| chr5:140691317-140691515 | Common:1; Rare:75; Clinvar:7 | ||||
| chr5:141320732-141320920 | Common:2; Rare:65 | ||||
| chr5:141636810-141637001 | Common:2; Rare:83 | ||||
| chr5:141682173-141682398 | Common:2; Rare:61 | ||||
| chr5:141923613-141923927 | Common:1; Rare:97 | ||||
| chr5:142012999-142013061 | Rare:19 |