| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9765480-9765820 | Rare:83 | ||||
| chr11:10599480-10599790 | Common:3; Rare:63 | ||||
| chr11:10604410-10604960 | Rare:162 | ||||
| chr11:10659351-10660033 | Common:6; Rare:179 | ||||
| chr11:12066158-12066558 | Common:16; Rare:198 | ||||
| chr11:12643000-12643390 | Common:2; Rare:106 | ||||
| chr11:13140330-13140790 | Common:4; Rare:167 | ||||
| chr11:16604222-16604622 | Common:7; Rare:187 | ||||
| chr11:17353640-17353960 | Common:8; Rare:153 | ||||
| chr11:19976547-19976760 | Common:2; Rare:78 | ||||
| chr11:19978730-19979020 | Rare:50 | ||||
| chr11:20002710-20003120 | Common:1; Rare:120 | ||||
| chr11:21752637-21753073 | Common:9; Rare:168 | ||||
| chr11:22624561-22625102 | Common:6; Rare:221; Clinvar:15; Clinvar (benign):12 | ||||
| chr11:26597137-26597432 | Common:5; Rare:60 |