| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140564550-140564858 | Rare:79 | ||||
| chr5:140639335-140639554 | Common:2; Rare:60 | ||||
| chr5:140646953-140647268 | Rare:73; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:140647277-140647442 | Rare:70; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr5:140647539-140648096 | Common:19; Rare:216; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:140648193-140648537 | Common:2; Rare:84 | ||||
| chr5:140664753-140664928 | Common:2; Rare:52 | ||||
| chr5:140675078-140675202 | Rare:35; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:140691309-140691653 | Common:1; Rare:123; Clinvar:10; Clinvar (benign):1 | ||||
| chr5:140693726-140693962 | Rare:62; Clinvar (benign):1 | ||||
| chr5:140700134-140700511 | Rare:113 | ||||
| chr5:140700636-140700922 | Common:1; Rare:64 | ||||
| chr5:140856289-140856607 | Rare:121 | ||||
| chr5:140870582-140870720 | Common:2; Rare:64 | ||||
| chr5:141094475-141094674 | Rare:44 |