| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43942164-43942243 | Rare:15 | ||||
| chr11:43942399-43942699 | Common:3; Rare:73 | ||||
| chr11:44065901-44066587 | Common:5; Rare:169 | ||||
| chr11:44095595-44095756 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr11:44309643-44310277 | Common:5; Rare:237; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr11:44310421-44310657 | Common:1; Rare:60 | ||||
| chr11:44565018-44565286 | Common:2; Rare:53 | ||||
| chr11:44565304-44565699 | Common:3; Rare:96 | ||||
| chr11:44949848-44950021 | Common:1; Rare:36 | ||||
| chr11:44950136-44950277 | Common:1; Rare:34 | ||||
| chr11:44950861-44951113 | Rare:61 | ||||
| chr11:45146222-45146301 | Rare:18 | ||||
| chr11:45146402-45146753 | Common:3; Rare:91 | ||||
| chr11:45146758-45146972 | Common:3; Rare:52 | ||||
| chr11:45147086-45147427 | Common:1; Rare:141 |