| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:52787547-52787760 | Common:5; Rare:46 | ||||
| chr5:52787823-52788280 | Common:2; Rare:92 | ||||
| chr5:53109711-53109921 | Common:1; Rare:106; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310426-54310711 | Common:1; Rare:84 | ||||
| chr5:54455580-54456105 | Common:2; Rare:165; Clinvar:6; Clinvar (benign):6 | ||||
| chr5:55307620-55308023 | Common:4; Rare:137 | ||||
| chr5:55534938-55535156 | Common:1; Rare:73 | ||||
| chr5:55994785-55995167 | Common:1; Rare:121 | ||||
| chr5:57173547-57173903 | Common:2; Rare:128 | ||||
| chr5:58460023-58460220 | Common:5; Rare:79 | ||||
| chr5:59039527-59039846 | Common:5; Rare:79 | ||||
| chr5:59356860-59357209 | Common:2; Rare:68 | ||||
| chr5:60700091-60700228 | Common:1; Rare:54 | ||||
| chr5:60945022-60945246 | Common:5; Rare:87; Clinvar:3; Clinvar (benign):5 | ||||
| chr5:61162332-61162637 | Common:1; Rare:78 |