| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:74640439-74640938 | Common:4; Rare:303 | ||||
| chr5:74641210-74641620 | Common:4; Rare:203 | ||||
| chr5:74685022-74685281 | Common:5; Rare:137; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:74767014-74767308 | Common:4; Rare:161 | ||||
| chr5:74866271-74866466 | Rare:119 | ||||
| chr5:74866754-74867016 | Common:2; Rare:83 | ||||
| chr5:75236868-75237064 | Common:9; Rare:121 | ||||
| chr5:75336854-75337321 | Common:9; Rare:299 | ||||
| chr5:75511593-75511917 | Common:2; Rare:227 | ||||
| chr5:75716940-75717190 | Common:2; Rare:92 | ||||
| chr5:75717349-75717682 | Common:10; Rare:167 | ||||
| chr5:76403101-76403471 | Common:3; Rare:154 | ||||
| chr5:76404070-76404486 | Common:7; Rare:97 | ||||
| chr5:76715738-76716235 | Common:15; Rare:220 | ||||
| chr5:76818762-76819118 | Common:3; Rare:96 |