| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18526874-18527040 | Common:2; Rare:79 | ||||
| chr11:18634332-18634566 | Common:2; Rare:74 | ||||
| chr11:19116947-19117189 | Common:3; Rare:64 | ||||
| chr11:20387417-20387786 | Common:7; Rare:119 | ||||
| chr11:22625179-22625244 | Common:1; Rare:21; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:22625813-22626028 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27363064-27363397 | Rare:148 | ||||
| chr11:27506705-27506903 | Common:1; Rare:91 | ||||
| chr11:28108106-28108451 | Common:2; Rare:104 | ||||
| chr11:30322918-30323195 | Common:3; Rare:79 | ||||
| chr11:31369737-31369888 | Rare:47 | ||||
| chr11:31509561-31509784 | Common:1; Rare:70 | ||||
| chr11:32583663-32583929 | Rare:95 | ||||
| chr11:33161448-33161600 | Common:5; Rare:42 | ||||
| chr11:33257133-33257427 | Common:3; Rare:94 |