| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:22192935-22193114 | Rare:40 | ||||
| chr11:22193270-22193322 | Common:4; Rare:6; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22625139-22625323 | Common:2; Rare:74; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:22625442-22625646 | Common:1; Rare:97; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr11:22625732-22626110 | Common:3; Rare:117; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:22666801-22667104 | Common:1; Rare:85 | ||||
| chr11:22668275-22668741 | Common:7; Rare:90 | ||||
| chr11:22672545-22672625 | Common:1; Rare:19 | ||||
| chr11:22829281-22829461 | Common:1; Rare:51 | ||||
| chr11:22829738-22830078 | Common:4; Rare:120 | ||||
| chr11:27363040-27363460 | Rare:174 | ||||
| chr11:27506691-27507003 | Common:1; Rare:127 | ||||
| chr11:27700445-27700609 | Common:2; Rare:38 | ||||
| chr11:28107833-28107901 | Rare:16 | ||||
| chr11:28108053-28108476 | Common:3; Rare:124 |