| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111912721-111912774 | Rare:4 | ||||
| chr11:111913132-111913289 | Rare:45 | ||||
| chr11:111923707-111923810 | Common:1; Rare:14 | ||||
| chr11:111936928-111937250 | Common:10; Rare:88 | ||||
| chr11:112025317-112025611 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:112073969-112074363 | Common:2; Rare:85 | ||||
| chr11:112086692-112086941 | Rare:112; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr11:112163999-112164081 | Common:2; Rare:17 | ||||
| chr11:112164083-112164422 | Common:1; Rare:60 | ||||
| chr11:112226257-112226669 | Common:1; Rare:160; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:113314453-113314608 | Rare:55 | ||||
| chr11:113875491-113875765 | Common:4; Rare:99 | ||||
| chr11:114059410-114060251 | Common:4; Rare:187 | ||||
| chr11:114296235-114296565 | Rare:62 | ||||
| chr11:114400007-114400071 | Rare:21 |