| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140691228-140691742 | Common:2; Rare:188; Clinvar:13; Clinvar (benign):4 | ||||
| chr5:140700280-140700488 | Rare:65 | ||||
| chr5:140794632-140794865 | Rare:40 | ||||
| chr5:140856436-140856697 | Rare:88 | ||||
| chr5:140875873-140876175 | Common:1; Rare:115 | ||||
| chr5:140882050-140882163 | Common:1; Rare:23 | ||||
| chr5:141172537-141172657 | Common:1; Rare:25 | ||||
| chr5:141320300-141320441 | Rare:37 | ||||
| chr5:141320692-141320933 | Common:3; Rare:85 | ||||
| chr5:141359885-141359981 | Rare:16 | ||||
| chr5:141413649-141413839 | Common:1; Rare:54 | ||||
| chr5:141484894-141485069 | Common:1; Rare:31 | ||||
| chr5:141636774-141637051 | Common:2; Rare:123 | ||||
| chr5:141637345-141637459 | Common:1; Rare:26 | ||||
| chr5:141682187-141682328 | Common:1; Rare:47 |