| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:33817997-33818208 | Common:1; Rare:94 | ||||
| chr13:34942164-34942294 | Common:3; Rare:39 | ||||
| chr13:36345551-36345583 | Rare:2 | ||||
| chr13:36346058-36346229 | Common:1; Rare:38 | ||||
| chr13:36346258-36346471 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346634-36346798 | Common:4; Rare:47 | ||||
| chr13:36999272-36999470 | Rare:80 | ||||
| chr13:37000259-37000457 | Common:2; Rare:41 | ||||
| chr13:37000518-37000805 | Common:3; Rare:90 | ||||
| chr13:37059585-37059754 | Common:1; Rare:55 | ||||
| chr13:38349520-38349932 | Common:4; Rare:141; Clinvar (pathogenic):1 | ||||
| chr13:38350208-38350533 | Common:2; Rare:94 | ||||
| chr13:38686774-38687109 | Common:4; Rare:93; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:39038087-39038531 | Common:1; Rare:105 | ||||
| chr13:39603120-39603284 | Common:1; Rare:55 |