| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10304875-10305088 | Common:1; Rare:48 | ||||
| chr11:10455068-10455445 | Common:5; Rare:63; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10456237-10456383 | Rare:34 | ||||
| chr11:10541122-10541464 | Common:3; Rare:103 | ||||
| chr11:10568452-10568716 | Common:1; Rare:66 | ||||
| chr11:10568723-10568915 | Rare:30 | ||||
| chr11:10750956-10751038 | Common:1; Rare:27 | ||||
| chr11:10751172-10751316 | Rare:44 | ||||
| chr11:10798996-10799388 | Common:3; Rare:135 | ||||
| chr11:10858007-10858279 | Common:3; Rare:89 | ||||
| chr11:11841753-11842095 | Common:4; Rare:107 | ||||
| chr11:11842192-11842217 | Rare:9 | ||||
| chr11:13463150-13463596 | Common:2; Rare:138 | ||||
| chr11:14520298-14520511 | Rare:73 | ||||
| chr11:16738466-16738769 | Common:3; Rare:69 |