| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47471989-47472241 | Rare:53 | ||||
| chr11:47487222-47487266 | Rare:7 | ||||
| chr11:47565273-47565486 | Rare:34 | ||||
| chr11:47565490-47565732 | Common:4; Rare:55 | ||||
| chr11:47578932-47579335 | Rare:191; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:47638699-47639051 | Common:5; Rare:91 | ||||
| chr11:47767214-47767690 | Common:2; Rare:160 | ||||
| chr11:57324860-57324991 | Common:1; Rare:39 | ||||
| chr11:57426451-57426703 | Common:2; Rare:46 | ||||
| chr11:57427030-57427214 | Common:1; Rare:57 | ||||
| chr11:57530677-57531071 | Common:1; Rare:95 | ||||
| chr11:57560345-57560576 | Rare:63 | ||||
| chr11:57567586-57567776 | Rare:61 | ||||
| chr11:57606132-57606464 | Rare:95; Clinvar (benign):1 | ||||
| chr11:57667733-57668186 | Common:5; Rare:147 |