| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:115975614-115975899 | Common:11; Rare:86 | ||||
| chr11:116733246-116733460 | Common:2; Rare:36 | ||||
| chr11:116734128-116734216 | Rare:19 | ||||
| chr11:116835552-116835573 | Rare:1 | ||||
| chr11:116835920-116836213 | Rare:114; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr11:117096559-117096748 | Rare:31 | ||||
| chr11:117610124-117610366 | Rare:54 | ||||
| chr11:117814330-117814610 | Common:3; Rare:53 | ||||
| chr11:117814731-117815124 | Common:4; Rare:99 | ||||
| chr11:117815379-117815855 | Common:3; Rare:90 | ||||
| chr11:117816496-117816747 | Common:3; Rare:58 | ||||
| chr11:117818143-117818451 | Common:2; Rare:72 | ||||
| chr11:117823963-117824210 | Common:1; Rare:30 | ||||
| chr11:117907258-117907509 | Common:3; Rare:57 | ||||
| chr11:117930728-117930798 | Common:1; Rare:12 |