| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36131570-36131604 | Rare:5 | ||||
| chr13:36297779-36297903 | Rare:44 | ||||
| chr13:36346270-36346558 | Common:3; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:36999260-36999410 | Rare:65 | ||||
| chr13:37000259-37000381 | Common:2; Rare:22 | ||||
| chr13:37000751-37000807 | Rare:25 | ||||
| chr13:37000985-37001071 | Rare:24 | ||||
| chr13:37001165-37001474 | Common:2; Rare:66 | ||||
| chr13:37059430-37059775 | Common:1; Rare:104 | ||||
| chr13:37869744-37869926 | Common:1; Rare:43 | ||||
| chr13:38349540-38350054 | Common:6; Rare:183; Clinvar (pathogenic):1 | ||||
| chr13:38350208-38350325 | Rare:47 | ||||
| chr13:39037714-39038056 | Common:1; Rare:106 | ||||
| chr13:39038064-39038426 | Common:1; Rare:92 | ||||
| chr13:39655557-39655803 | Common:4; Rare:124; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 |