| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30307001-30307160 | Common:3; Rare:34 | ||||
| chr13:30465795-30466119 | Common:1; Rare:103 | ||||
| chr13:30617577-30617993 | Common:1; Rare:126 | ||||
| chr13:31162337-31162425 | Common:1; Rare:21 | ||||
| chr13:32031630-32031777 | Common:1; Rare:43 | ||||
| chr13:32586219-32586579 | Common:2; Rare:107 | ||||
| chr13:33285765-33285861 | Rare:20 | ||||
| chr13:35855530-35855849 | Common:1; Rare:71 | ||||
| chr13:36297708-36297978 | Common:1; Rare:99 | ||||
| chr13:36345543-36345671 | Common:1; Rare:25 | ||||
| chr13:36346576-36346889 | Common:4; Rare:85 | ||||
| chr13:37000179-37000404 | Common:2; Rare:45 | ||||
| chr13:37000452-37000815 | Common:3; Rare:116; Clinvar (pathogenic):1 | ||||
| chr13:37059578-37059751 | Common:1; Rare:58 | ||||
| chr13:38686814-38687129 | Common:3; Rare:94; Clinvar:3; Clinvar (benign):1 |