| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18526835-18527040 | Common:2; Rare:103 | ||||
| chr11:18588650-18588929 | Common:3; Rare:98 | ||||
| chr11:18634278-18634570 | Common:3; Rare:101 | ||||
| chr11:18634773-18634828 | Rare:17 | ||||
| chr11:18698688-18698803 | Common:3; Rare:33 | ||||
| chr11:18791546-18791857 | Common:1; Rare:102 | ||||
| chr11:20387417-20387771 | Common:7; Rare:115 | ||||
| chr11:20668930-20669134 | Common:2; Rare:62 | ||||
| chr11:22337609-22337676 | Rare:13 | ||||
| chr11:22337778-22337906 | Common:1; Rare:23 | ||||
| chr11:22337909-22338024 | Common:1; Rare:25 | ||||
| chr11:22338186-22338618 | Common:1; Rare:117 | ||||
| chr11:22625507-22625609 | Rare:50; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625806-22626002 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:22829357-22829414 | Common:1; Rare:17 |