| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:133130287-133130611 | Common:7; Rare:102 | ||||
| chr13:19863512-19863969 | Common:6; Rare:171 | ||||
| chr13:20525766-20525962 | Common:1; Rare:75 | ||||
| chr13:21176491-21176696 | Common:1; Rare:90 | ||||
| chr13:23579241-23579400 | Common:3; Rare:50 | ||||
| chr13:23889289-23889591 | Common:1; Rare:104 | ||||
| chr13:24512727-24512813 | Common:1; Rare:25 | ||||
| chr13:27450133-27450222 | Common:3; Rare:27 | ||||
| chr13:27620601-27620757 | Common:1; Rare:35 | ||||
| chr13:30306809-30307197 | Common:7; Rare:103 | ||||
| chr13:32586256-32586585 | Common:2; Rare:101 | ||||
| chr13:35476322-35476749 | Common:1; Rare:75 | ||||
| chr13:36346289-36346519 | Common:3; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:36999300-36999468 | Rare:65 | ||||
| chr13:37000219-37000404 | Common:2; Rare:34 |