| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:147782708-147782889 | Rare:44 | ||||
| chr5:147906493-147906630 | Common:1; Rare:34 | ||||
| chr5:148383723-148384033 | Rare:81 | ||||
| chr5:149063010-149063584 | Common:1; Rare:112; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr5:149141386-149141768 | Rare:103 | ||||
| chr5:149271716-149271912 | Common:1; Rare:61 | ||||
| chr5:149345327-149345673 | Common:3; Rare:128 | ||||
| chr5:149550906-149551076 | Rare:41 | ||||
| chr5:149551202-149551656 | Common:2; Rare:105 | ||||
| chr5:149581245-149581583 | Common:2; Rare:81 | ||||
| chr5:149960535-149960937 | Common:1; Rare:142; Clinvar:7 | ||||
| chr5:150357513-150357759 | Rare:74; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:150412693-150412827 | Common:1; Rare:34 | ||||
| chr5:150449646-150449810 | Common:4; Rare:56 | ||||
| chr5:150485902-150485946 | Common:1; Rare:7 |