| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:56952432-56952832 | Common:5; Rare:111 | ||||
| chr5:57173543-57174091 | Common:3; Rare:191 | ||||
| chr5:57174361-57174761 | Common:2; Rare:145 | ||||
| chr5:58460049-58460188 | Common:3; Rare:57 | ||||
| chr5:58582033-58582182 | Common:1; Rare:31 | ||||
| chr5:58582872-58583211 | Common:2; Rare:92 | ||||
| chr5:58999780-59000180 | Rare:128 | ||||
| chr5:59768640-59768759 | Rare:36 | ||||
| chr5:60699728-60699938 | Common:2; Rare:37 | ||||
| chr5:60700098-60700301 | Common:4; Rare:82 | ||||
| chr5:60944998-60945238 | Common:5; Rare:98; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:61162255-61162583 | Common:1; Rare:81 | ||||
| chr5:61331627-61331829 | Common:3; Rare:87 | ||||
| chr5:61332011-61332271 | Rare:96 | ||||
| chr5:61332625-61333515 | Common:20; Rare:408; Clinvar:2 |