| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:42048913-42049289 | Common:3; Rare:78 | ||||
| chr13:42271554-42272337 | Common:7; Rare:201 | ||||
| chr13:42272339-42272735 | Common:6; Rare:96 | ||||
| chr13:42573992-42574180 | Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:42574230-42574366 | Rare:46; Clinvar:3 | ||||
| chr13:42574577-42574763 | Common:1; Rare:37 | ||||
| chr13:42991768-42992035 | Common:1; Rare:81 | ||||
| chr13:42992118-42992501 | Common:3; Rare:91 | ||||
| chr13:42992682-42992850 | Rare:26 | ||||
| chr13:43023342-43023888 | Common:7; Rare:200 | ||||
| chr13:43879010-43879167 | Common:1; Rare:32 | ||||
| chr13:43879422-43880175 | Common:21; Rare:174 | ||||
| chr13:44435170-44435473 | Common:3; Rare:88 | ||||
| chr13:44436827-44437003 | Common:2; Rare:56 | ||||
| chr13:44575995-44576194 | Common:1; Rare:74 |