| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10858013-10858309 | Common:3; Rare:95 | ||||
| chr11:11621965-11622241 | Common:4; Rare:110 | ||||
| chr11:11841940-11842077 | Common:1; Rare:38 | ||||
| chr11:13463159-13463336 | Common:1; Rare:64 | ||||
| chr11:14643631-14643720 | Common:1; Rare:45 | ||||
| chr11:16738466-16738725 | Common:3; Rare:56 | ||||
| chr11:17077595-17077805 | Common:2; Rare:86 | ||||
| chr11:17207905-17208111 | Common:2; Rare:80 | ||||
| chr11:18322108-18322321 | Common:4; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322496-18322607 | Common:2; Rare:50 | ||||
| chr11:18526840-18526987 | Rare:73 | ||||
| chr11:18588661-18588815 | Rare:57 | ||||
| chr11:20363689-20363748 | Rare:13 | ||||
| chr11:22625524-22625591 | Rare:32; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626006 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 |