| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112073943-112074344 | Common:2; Rare:88 | ||||
| chr11:112086696-112086899 | Rare:89 | ||||
| chr11:112175603-112176003 | Common:1; Rare:92 | ||||
| chr11:112226259-112226691 | Common:1; Rare:168; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961144-112961446 | Common:2; Rare:117 | ||||
| chr11:113314386-113314702 | Common:1; Rare:100 | ||||
| chr11:113706220-113706650 | Common:2; Rare:76 | ||||
| chr11:113773635-113773882 | Common:1; Rare:75 | ||||
| chr11:113875457-113875828 | Common:4; Rare:139 | ||||
| chr11:114059382-114059749 | Rare:80 | ||||
| chr11:114060206-114060548 | Common:2; Rare:66 | ||||
| chr11:114256956-114257993 | Common:3; Rare:284 | ||||
| chr11:114400358-114400717 | Common:2; Rare:140 | ||||
| chr11:114439290-114439509 | Common:1; Rare:63 | ||||
| chr11:114439800-114440180 | Rare:122 |