| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:149501446-149501892 | Common:2; Rare:83 | ||||
| chr5:149550354-149550387 | Rare:7 | ||||
| chr5:149550842-149550968 | Rare:21 | ||||
| chr5:149551353-149551645 | Rare:69 | ||||
| chr5:149960575-149960974 | Rare:133; Clinvar:8 | ||||
| chr5:150302811-150302896 | Rare:18 | ||||
| chr5:150379015-150379718 | Common:3; Rare:213; Clinvar:4; Clinvar (benign):6 | ||||
| chr5:150447377-150447396 | Common:1; Rare:6 | ||||
| chr5:150449613-150449795 | Common:4; Rare:57 | ||||
| chr5:150485504-150485965 | Common:5; Rare:94 | ||||
| chr5:150486023-150486348 | Common:2; Rare:67 | ||||
| chr5:150700962-150701114 | Common:2; Rare:64 | ||||
| chr5:150904777-150905260 | Common:4; Rare:112 | ||||
| chr5:151080880-151081204 | Common:1; Rare:101 | ||||
| chr5:151253100-151253271 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 |