| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:50667781-50667897 | Common:1; Rare:37 | ||||
| chr5:51383242-51383448 | Common:2; Rare:80 | ||||
| chr5:53109716-53109899 | Common:1; Rare:95; Clinvar:3 | ||||
| chr5:53560614-53560692 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:54310513-54310711 | Rare:63 | ||||
| chr5:55233606-55233897 | Common:4; Rare:106 | ||||
| chr5:55307631-55308016 | Common:4; Rare:130 | ||||
| chr5:55534571-55534923 | Common:3; Rare:98 | ||||
| chr5:55534956-55535211 | Common:1; Rare:86 | ||||
| chr5:55737904-55738083 | Common:2; Rare:45 | ||||
| chr5:55994807-55995184 | Rare:128 | ||||
| chr5:57173601-57174125 | Common:2; Rare:176 | ||||
| chr5:60488002-60488370 | Common:1; Rare:64 | ||||
| chr5:60700129-60700226 | Common:1; Rare:29 | ||||
| chr5:60945001-60945229 | Common:5; Rare:93; Clinvar:4; Clinvar (benign):5 |