| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131929054-131929327 | Common:9; Rare:84; Clinvar:1 | ||||
| chr12:132144306-132144486 | Rare:73 | ||||
| chr12:132687329-132687623 | Common:2; Rare:105; Clinvar:2; Clinvar (benign):7 | ||||
| chr12:132956262-132956370 | Common:1; Rare:26 | ||||
| chr13:20566942-20567201 | Common:1; Rare:88 | ||||
| chr13:21176524-21176698 | Common:1; Rare:80 | ||||
| chr13:23889303-23889541 | Common:1; Rare:86 | ||||
| chr13:24512738-24512847 | Common:3; Rare:34 | ||||
| chr13:27251253-27251619 | Common:5; Rare:109 | ||||
| chr13:27424545-27424707 | Common:2; Rare:53 | ||||
| chr13:28659061-28659184 | Rare:53; Clinvar (pathogenic):1 | ||||
| chr13:30307049-30307181 | Common:1; Rare:20 | ||||
| chr13:30307383-30307603 | Common:2; Rare:75 | ||||
| chr13:36346275-36346513 | Common:3; Rare:67; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:37000756-37000801 | Rare:22 |