| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32315332-32315721 | Common:2; Rare:100; Clinvar:4; Clinvar (benign):6 | ||||
| chr13:32315739-32316238 | Common:4; Rare:119; Clinvar (benign):5 | ||||
| chr13:32316315-32316357 | Rare:3 | ||||
| chr13:32428122-32428179 | Rare:10 | ||||
| chr13:32538114-32538550 | Common:1; Rare:93 | ||||
| chr13:32538686-32538978 | Common:1; Rare:77 | ||||
| chr13:32586181-32586660 | Common:2; Rare:144 | ||||
| chr13:32586869-32587175 | Common:5; Rare:97 | ||||
| chr13:33016453-33016535 | Common:1; Rare:17 | ||||
| chr13:33205919-33206180 | Rare:51 | ||||
| chr13:33285673-33286016 | Common:1; Rare:71 | ||||
| chr13:33350056-33350202 | Rare:40 | ||||
| chr13:33817966-33818268 | Common:2; Rare:134 | ||||
| chr13:33818555-33818726 | Rare:44 | ||||
| chr13:34941869-34941982 | Rare:20 |