| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36131318-36131520 | Rare:51 | ||||
| chr13:36297787-36297909 | Rare:43 | ||||
| chr13:36346301-36346454 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:37059578-37059726 | Common:1; Rare:52 | ||||
| chr13:37869621-37869894 | Common:1; Rare:72 | ||||
| chr13:38349541-38349924 | Common:4; Rare:131; Clinvar (pathogenic):1 | ||||
| chr13:38350255-38350336 | Rare:27 | ||||
| chr13:39038012-39038482 | Common:1; Rare:120 | ||||
| chr13:39655633-39655802 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40771078-40771268 | Common:1; Rare:76 | ||||
| chr13:41061188-41061665 | Common:3; Rare:167 | ||||
| chr13:41132331-41132502 | Common:1; Rare:51 | ||||
| chr13:41132677-41132971 | Rare:73 | ||||
| chr13:41194460-41194659 | Common:2; Rare:48 | ||||
| chr13:42271760-42272033 | Common:2; Rare:78 |