| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36346084-36346478 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):3 | ||||
| chr13:36346622-36346782 | Common:4; Rare:46 | ||||
| chr13:36999254-36999457 | Rare:84 | ||||
| chr13:37000736-37000808 | Rare:29 | ||||
| chr13:37059596-37059751 | Common:1; Rare:52 | ||||
| chr13:37598597-37598885 | Common:2; Rare:84 | ||||
| chr13:37869759-37869882 | Common:1; Rare:28 | ||||
| chr13:38349541-38349919 | Common:4; Rare:128; Clinvar (pathogenic):1 | ||||
| chr13:38350214-38350474 | Common:1; Rare:79 | ||||
| chr13:38686896-38687111 | Common:3; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:39038064-39038532 | Common:1; Rare:110 | ||||
| chr13:39655608-39655802 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40771138-40771264 | Common:1; Rare:44 | ||||
| chr13:40789377-40789621 | Common:2; Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:40982858-40983035 | Common:3; Rare:28 |