| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27251213-27251599 | Common:7; Rare:126 | ||||
| chr13:27270696-27270830 | Rare:44 | ||||
| chr13:28658911-28659187 | Rare:113; Clinvar (pathogenic):1 | ||||
| chr13:30306999-30307197 | Common:4; Rare:47 | ||||
| chr13:30307401-30307623 | Common:2; Rare:73 | ||||
| chr13:30617255-30617993 | Common:1; Rare:226 | ||||
| chr13:32586275-32586582 | Common:2; Rare:92 | ||||
| chr13:33285710-33286002 | Common:1; Rare:61 | ||||
| chr13:36346269-36346454 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36370304-36370359 | Rare:19 | ||||
| chr13:37000748-37000805 | Rare:25 | ||||
| chr13:37059620-37059726 | Common:1; Rare:34 | ||||
| chr13:41060924-41061068 | Common:10; Rare:74 | ||||
| chr13:41061144-41061570 | Common:4; Rare:146 | ||||
| chr13:43879467-43879585 | Rare:34 |