| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75549480-75549823 | Common:8; Rare:85 | ||||
| chr13:76992024-76992188 | Common:1; Rare:73; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr13:77027137-77027274 | Common:5; Rare:45 | ||||
| chr13:77327054-77327333 | Common:1; Rare:103 | ||||
| chr13:77918729-77918932 | Common:1; Rare:45 | ||||
| chr13:79405795-79405889 | Rare:33 | ||||
| chr13:79406219-79406314 | Common:1; Rare:29 | ||||
| chr13:80338894-80339072 | Rare:42 | ||||
| chr13:80339300-80339331 | Common:1; Rare:4 | ||||
| chr13:80340789-80340811 | Rare:6 | ||||
| chr13:80340822-80340846 | Rare:4 | ||||
| chr13:93226778-93226878 | Common:1; Rare:21; Clinvar (benign):1 | ||||
| chr13:93227042-93227576 | Common:2; Rare:140; Clinvar:7; Clinvar (benign):2 | ||||
| chr13:94596139-94596334 | Common:2; Rare:63 | ||||
| chr13:94601606-94601936 | Common:3; Rare:103 |