| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36919717-36919761 | Rare:15 | ||||
| chr13:36919912-36920003 | Common:1; Rare:30 | ||||
| chr13:36920092-36920449 | Common:8; Rare:148; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:36999198-36999473 | Rare:114 | ||||
| chr13:36999906-37000063 | Common:1; Rare:43 | ||||
| chr13:37000217-37000415 | Common:2; Rare:36 | ||||
| chr13:37000495-37000961 | Common:4; Rare:156; Clinvar (pathogenic):1 | ||||
| chr13:37000970-37001129 | Rare:37 | ||||
| chr13:37001390-37001435 | Common:2; Rare:14 | ||||
| chr13:37001466-37001514 | Rare:10 | ||||
| chr13:37001773-37002112 | Common:1; Rare:70 | ||||
| chr13:37058953-37059050 | Rare:21 | ||||
| chr13:37059183-37059275 | Rare:13 | ||||
| chr13:37059537-37059822 | Common:2; Rare:103 | ||||
| chr13:37869271-37869331 | Rare:7 |