| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111602829-111603123 | Rare:66 | ||||
| chr11:111765931-111765994 | Rare:14 | ||||
| chr11:111766121-111766161 | Common:1; Rare:11 | ||||
| chr11:111766272-111766493 | Common:3; Rare:122 | ||||
| chr11:111766632-111766913 | Rare:63 | ||||
| chr11:111814608-111814922 | Common:1; Rare:47 | ||||
| chr11:111871028-111871056 | Rare:7 | ||||
| chr11:111871436-111871680 | Rare:79; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:111878614-111878663 | Common:1; Rare:10 | ||||
| chr11:111878878-111879125 | Common:3; Rare:103 | ||||
| chr11:111879135-111879359 | Rare:80 | ||||
| chr11:111879442-111879577 | Common:1; Rare:49 | ||||
| chr11:111914185-111914365 | Common:1; Rare:32 | ||||
| chr11:111918894-111919007 | Rare:31 | ||||
| chr11:111923408-111923464 | Rare:11 |