| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58668367-58668477 | Rare:20 | ||||
| chr17:58679622-58679959 | Rare:143 | ||||
| chr17:58696610-58697090 | Common:2; Rare:253; Clinvar:58; Clinvar (benign):34; Clinvar (pathogenic):12 | ||||
| chr17:58914317-58914417 | Rare:18 | ||||
| chr17:59026640-59026892 | Rare:49 | ||||
| chr17:59062550-59062850 | Common:2; Rare:104; Clinvar (benign):2 | ||||
| chr17:59083852-59084252 | Rare:96; Clinvar (pathogenic):2 | ||||
| chr17:59087291-59087831 | Common:5; Rare:157 | ||||
| chr17:59090295-59090951 | Common:9; Rare:290 | ||||
| chr17:59114359-59115379 | Common:3; Rare:199 | ||||
| chr17:59115505-59116418 | Common:4; Rare:238 | ||||
| chr17:59116786-59117190 | Common:2; Rare:119 | ||||
| chr17:59117264-59117738 | Common:3; Rare:123 | ||||
| chr17:59118467-59119157 | Common:3; Rare:181 | ||||
| chr17:59120031-59120447 | Common:3; Rare:136 |