| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27621094-27621136 | Common:1; Rare:11 | ||||
| chr13:28138127-28138234 | Common:1; Rare:34 | ||||
| chr13:28659071-28659184 | Rare:48; Clinvar (pathogenic):1 | ||||
| chr13:30306832-30307197 | Common:6; Rare:98 | ||||
| chr13:30307388-30307483 | Common:2; Rare:36 | ||||
| chr13:30617327-30618039 | Common:1; Rare:227 | ||||
| chr13:32031217-32031336 | Common:1; Rare:34 | ||||
| chr13:32315361-32315538 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:32428053-32428205 | Rare:37 | ||||
| chr13:33285662-33285885 | Rare:51 | ||||
| chr13:33350577-33350803 | Rare:60 | ||||
| chr13:35476317-35476841 | Common:1; Rare:92 | ||||
| chr13:35855595-35855842 | Common:1; Rare:54 | ||||
| chr13:36346258-36346468 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:37059596-37059751 | Common:1; Rare:52 |