| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102347111-102347336 | Common:2; Rare:76 | ||||
| chr11:102452526-102452905 | Common:1; Rare:126 | ||||
| chr11:103092024-103092261 | Common:1; Rare:72 | ||||
| chr11:105045308-105045430 | Rare:35 | ||||
| chr11:106077313-106077706 | Common:2; Rare:118 | ||||
| chr11:108009306-108009349 | Rare:23 | ||||
| chr11:108222609-108223115 | Common:1; Rare:158; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:111602224-111602572 | Common:1; Rare:114 | ||||
| chr11:111766332-111766459 | Common:1; Rare:81 | ||||
| chr11:111879158-111879541 | Rare:113 | ||||
| chr11:111912718-111912757 | Rare:5 | ||||
| chr11:111913138-111913298 | Rare:45 | ||||
| chr11:112073995-112074358 | Common:1; Rare:75 | ||||
| chr11:112086667-112086918 | Rare:113; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:112226314-112226475 | Rare:72 |