| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:33205992-33206142 | Rare:32 | ||||
| chr13:33285652-33285887 | Rare:56 | ||||
| chr13:33818013-33818276 | Common:1; Rare:117 | ||||
| chr13:34942178-34942294 | Common:2; Rare:36 | ||||
| chr13:35476647-35476841 | Common:1; Rare:30 | ||||
| chr13:36345538-36345671 | Common:1; Rare:25 | ||||
| chr13:36346240-36346466 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346622-36346787 | Common:4; Rare:46 | ||||
| chr13:36346890-36346930 | Rare:10 | ||||
| chr13:37000259-37000407 | Common:2; Rare:27 | ||||
| chr13:37000743-37000808 | Rare:28 | ||||
| chr13:37059458-37059737 | Common:1; Rare:81 | ||||
| chr13:37869755-37869892 | Common:1; Rare:32 | ||||
| chr13:38350241-38350474 | Common:1; Rare:68 | ||||
| chr13:39038087-39038567 | Common:1; Rare:117 |