| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:141923726-141923927 | Common:1; Rare:62 | ||||
| chr5:142012986-142013120 | Rare:40 | ||||
| chr5:142108715-142108977 | Common:2; Rare:89 | ||||
| chr5:142324965-142325157 | Rare:75 | ||||
| chr5:143404419-143404537 | Rare:28 | ||||
| chr5:144170563-144170852 | Common:2; Rare:93 | ||||
| chr5:146182500-146182856 | Common:3; Rare:98 | ||||
| chr5:146203309-146203634 | Common:2; Rare:97 | ||||
| chr5:146878734-146878767 | Rare:12 | ||||
| chr5:147509746-147509846 | Rare:22 | ||||
| chr5:147509861-147510074 | Rare:58 | ||||
| chr5:148383828-148384013 | Rare:52 | ||||
| chr5:149063020-149063399 | Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:149141397-149141526 | Rare:37 | ||||
| chr5:149345363-149345529 | Common:1; Rare:54 |