| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:77027120-77027289 | Common:5; Rare:55 | ||||
| chr13:77326968-77327305 | Common:1; Rare:135 | ||||
| chr13:77918663-77918934 | Common:2; Rare:58 | ||||
| chr13:77919397-77919696 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:79405734-79405909 | Common:1; Rare:59 | ||||
| chr13:79406217-79406339 | Common:3; Rare:38 | ||||
| chr13:79481024-79481479 | Common:2; Rare:178 | ||||
| chr13:80341303-80341478 | Rare:55 | ||||
| chr13:94712514-94712729 | Common:2; Rare:43 | ||||
| chr13:94712754-94712852 | Common:2; Rare:25 | ||||
| chr13:95676911-95677229 | Common:3; Rare:113 | ||||
| chr13:96053369-96053542 | Common:2; Rare:69 | ||||
| chr13:97222154-97222450 | Rare:51 | ||||
| chr13:98576172-98576321 | Common:1; Rare:51 | ||||
| chr13:99200661-99200915 | Common:6; Rare:117 |