| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123062550-123063219 | Common:4; Rare:238 | ||||
| chr11:123063256-123063525 | Common:1; Rare:64 | ||||
| chr11:123063667-123063745 | Common:1; Rare:9 | ||||
| chr11:123083708-123083827 | Common:1; Rare:30; Clinvar (pathogenic):1 | ||||
| chr11:123194703-123195282 | Common:4; Rare:143 | ||||
| chr11:123195285-123195485 | Common:2; Rare:36 | ||||
| chr11:123195709-123195787 | Rare:15 | ||||
| chr11:123454351-123454515 | Common:1; Rare:27 | ||||
| chr11:123654136-123654207 | Rare:16; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:123654326-123654418 | Rare:21; Clinvar:2 | ||||
| chr11:123654522-123654787 | Common:5; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:123741238-123741495 | Rare:59 | ||||
| chr11:123741507-123741831 | Common:2; Rare:83 | ||||
| chr11:123978043-123978250 | Common:1; Rare:28 | ||||
| chr11:124622723-124623009 | Common:5; Rare:92 |