| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111937090-111937439 | Common:7; Rare:100 | ||||
| chr11:112025293-112025464 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:112074005-112074351 | Common:1; Rare:72 | ||||
| chr11:112086722-112086905 | Rare:76; Clinvar:1 | ||||
| chr11:112226314-112226443 | Rare:61 | ||||
| chr11:112961353-112961525 | Rare:74 | ||||
| chr11:113314414-113314598 | Rare:65 | ||||
| chr11:113875479-113875762 | Common:4; Rare:100 | ||||
| chr11:114059421-114059734 | Rare:67 | ||||
| chr11:114400421-114400740 | Common:2; Rare:131 | ||||
| chr11:117199141-117199385 | Common:4; Rare:73 | ||||
| chr11:117986225-117986405 | Common:4; Rare:56; Clinvar:1 | ||||
| chr11:118264284-118264593 | Common:1; Rare:50 | ||||
| chr11:118359427-118359647 | Common:3; Rare:96 | ||||
| chr11:118401340-118401661 | Rare:105 |