| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111879154-111879541 | Rare:115 | ||||
| chr11:111911948-111912158 | Common:3; Rare:42 | ||||
| chr11:111912708-111912774 | Rare:6 | ||||
| chr11:111913138-111913275 | Rare:40 | ||||
| chr11:111937129-111937225 | Common:4; Rare:36 | ||||
| chr11:112073987-112074377 | Common:1; Rare:86 | ||||
| chr11:112086719-112086910 | Rare:79; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:112167242-112167357 | Common:1; Rare:35 | ||||
| chr11:112226285-112226446 | Rare:71 | ||||
| chr11:112226597-112226669 | Common:1; Rare:23 | ||||
| chr11:113314454-113314602 | Rare:51 | ||||
| chr11:113875491-113875765 | Common:4; Rare:99 | ||||
| chr11:114059410-114059740 | Rare:73 | ||||
| chr11:114296251-114296559 | Rare:56 | ||||
| chr11:114400405-114400753 | Common:2; Rare:135 |