| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112025306-112025552 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:112073991-112074343 | Common:1; Rare:74 | ||||
| chr11:112086691-112086911 | Rare:99; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr11:112164029-112164198 | Rare:32 | ||||
| chr11:112175221-112175539 | Common:1; Rare:57 | ||||
| chr11:112226238-112226711 | Common:1; Rare:176; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:113314380-113314717 | Common:1; Rare:106 | ||||
| chr11:113387830-113388301 | Common:2; Rare:230 | ||||
| chr11:113773647-113773886 | Common:1; Rare:75 | ||||
| chr11:113875472-113875836 | Common:4; Rare:136 | ||||
| chr11:113975025-113975209 | Rare:55 | ||||
| chr11:114400333-114400633 | Common:2; Rare:103 | ||||
| chr11:114439287-114439519 | Common:1; Rare:68 | ||||
| chr11:114439810-114440380 | Rare:153 | ||||
| chr11:116772714-116773147 | Common:3; Rare:151 |