| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112073987-112074363 | Common:1; Rare:81 | ||||
| chr11:112086729-112086917 | Rare:77; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:112226298-112226650 | Common:1; Rare:147; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961326-112961638 | Common:4; Rare:151 | ||||
| chr11:113314448-113314579 | Rare:42 | ||||
| chr11:113875497-113875771 | Common:4; Rare:101 | ||||
| chr11:114059400-114059764 | Rare:78 | ||||
| chr11:114400455-114400723 | Common:2; Rare:111 | ||||
| chr11:115504368-115504640 | Common:2; Rare:83 | ||||
| chr11:116772975-116773036 | Rare:16 | ||||
| chr11:117144188-117144370 | Common:2; Rare:94 | ||||
| chr11:117316257-117316418 | Common:1; Rare:33 | ||||
| chr11:117797139-117797341 | Common:1; Rare:80 | ||||
| chr11:117876593-117876806 | Rare:61 | ||||
| chr11:117986324-117986415 | Common:2; Rare:27; Clinvar:2 |