| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:44565029-44565245 | Common:2; Rare:45 | ||||
| chr11:44565248-44565752 | Common:3; Rare:127 | ||||
| chr11:44950150-44950214 | Common:1; Rare:20 | ||||
| chr11:44950637-44950795 | Rare:41 | ||||
| chr11:44950845-44950964 | Rare:25 | ||||
| chr11:45146184-45146301 | Rare:26 | ||||
| chr11:45146409-45146980 | Common:6; Rare:152 | ||||
| chr11:45147060-45147398 | Common:1; Rare:142 | ||||
| chr11:45804236-45804473 | Common:1; Rare:52 | ||||
| chr11:45804530-45804611 | Rare:19 | ||||
| chr11:45804906-45805252 | Common:3; Rare:93; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:45805337-45805521 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:45847179-45847545 | Common:2; Rare:155 | ||||
| chr11:45885641-45885693 | Rare:15 | ||||
| chr11:45907250-45907274 | Rare:12 |