| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140564573-140564837 | Rare:73 | ||||
| chr5:140647589-140647921 | Common:5; Rare:135; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664742-140664904 | Common:3; Rare:39 | ||||
| chr5:140691309-140691504 | Common:1; Rare:74; Clinvar:7 | ||||
| chr5:140794673-140794874 | Rare:34 | ||||
| chr5:140800970-140801109 | Common:2; Rare:20 | ||||
| chr5:140834239-140834269 | Rare:5 | ||||
| chr5:140868673-140868987 | Common:2; Rare:72 | ||||
| chr5:141172537-141172684 | Common:1; Rare:27 | ||||
| chr5:141320742-141320920 | Common:1; Rare:62 | ||||
| chr5:141484707-141485069 | Common:2; Rare:69 | ||||
| chr5:141636810-141637011 | Common:2; Rare:86 | ||||
| chr5:141923740-141923914 | Common:1; Rare:52 | ||||
| chr5:142013001-142013129 | Rare:39 | ||||
| chr5:142324973-142325238 | Rare:89 |