| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:50667768-50667912 | Common:1; Rare:45 | ||||
| chr5:53109716-53109903 | Common:1; Rare:96; Clinvar:3 | ||||
| chr5:54310507-54310711 | Rare:65 | ||||
| chr5:55307611-55308044 | Common:5; Rare:155 | ||||
| chr5:55994880-55995199 | Rare:116 | ||||
| chr5:57173727-57174132 | Common:1; Rare:141 | ||||
| chr5:58460038-58460246 | Common:5; Rare:86 | ||||
| chr5:58582903-58583211 | Common:2; Rare:81 | ||||
| chr5:60488014-60488218 | Common:1; Rare:30 | ||||
| chr5:60700084-60700249 | Common:1; Rare:63 | ||||
| chr5:60844183-60844406 | Common:5; Rare:78 | ||||
| chr5:60945031-60945276 | Common:4; Rare:92; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:61162254-61162481 | Rare:42 | ||||
| chr5:62306134-62306535 | Common:3; Rare:146; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:62403859-62404030 | Common:3; Rare:57 |