| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:533568-533651 | Rare:41; Clinvar:3; Clinvar (benign):6 | ||||
| chr11:537303-537546 | Common:5; Rare:76 | ||||
| chr11:560701-561028 | Common:7; Rare:151 | ||||
| chr11:576422-576584 | Rare:67 | ||||
| chr11:601381-601526 | Common:2; Rare:34 | ||||
| chr11:615936-616027 | Rare:27 | ||||
| chr11:695731-695830 | Rare:33 | ||||
| chr11:706020-706263 | Common:2; Rare:80 | ||||
| chr11:706511-706646 | Rare:22 | ||||
| chr11:720574-720909 | Common:1; Rare:126 | ||||
| chr11:747309-747575 | Rare:113; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:763170-763509 | Common:23; Rare:174; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr11:763986-764430 | Common:4; Rare:119; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:764654-764844 | Common:1; Rare:69; Clinvar:1 | ||||
| chr11:777449-777614 | Common:1; Rare:74 |