| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36345545-36345840 | Common:2; Rare:68 | ||||
| chr13:36346073-36346252 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr13:36346260-36346459 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346560-36346835 | Common:4; Rare:74 | ||||
| chr13:36920036-36920108 | Common:1; Rare:23 | ||||
| chr13:36999257-36999458 | Rare:83 | ||||
| chr13:37000227-37000427 | Common:2; Rare:37 | ||||
| chr13:37000526-37000815 | Common:3; Rare:95; Clinvar (pathogenic):1 | ||||
| chr13:37059449-37059739 | Common:1; Rare:84 | ||||
| chr13:37869145-37869377 | Common:1; Rare:39 | ||||
| chr13:37869631-37869936 | Common:1; Rare:81 | ||||
| chr13:37870338-37870428 | Common:1; Rare:24 | ||||
| chr13:38349450-38349559 | Common:1; Rare:29 | ||||
| chr13:38686862-38687117 | Common:3; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:39037466-39037652 | Common:1; Rare:55 |