| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:72252749-72252796 | Rare:10 | ||||
| chr11:72280824-72280935 | Common:1; Rare:25 | ||||
| chr11:72301816-72302117 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:72302292-72302609 | Common:1; Rare:66; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr11:72343712-72344022 | Common:3; Rare:46 | ||||
| chr11:72351187-72351334 | Rare:20 | ||||
| chr11:72352564-72352725 | Rare:19 | ||||
| chr11:73182853-73183143 | Common:1; Rare:59 | ||||
| chr11:73598915-73599092 | Common:1; Rare:27 | ||||
| chr11:74845239-74845495 | Common:1; Rare:59 | ||||
| chr11:75098702-75099029 | Common:3; Rare:78 | ||||
| chr11:76284267-76284439 | Common:3; Rare:28 | ||||
| chr11:76328193-76328325 | Common:1; Rare:18 | ||||
| chr11:76593134-76593268 | Rare:20 | ||||
| chr11:77748910-77749058 | Rare:23 |