| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61789410-61789448 | Rare:3 | ||||
| chr11:62140800-62141012 | Common:1; Rare:70 | ||||
| chr11:62500314-62500634 | Common:1; Rare:63 | ||||
| chr11:62630382-62630765 | Rare:114 | ||||
| chr11:62711732-62711952 | Common:1; Rare:29 | ||||
| chr11:62764843-62765209 | Common:4; Rare:85 | ||||
| chr11:62765215-62765721 | Common:2; Rare:132 | ||||
| chr11:62766245-62766553 | Common:6; Rare:71 | ||||
| chr11:62852006-62852115 | Common:1; Rare:29 | ||||
| chr11:62852330-62852442 | Rare:29 | ||||
| chr11:62852508-62852620 | Common:1; Rare:35 | ||||
| chr11:63244386-63244641 | Common:1; Rare:49 | ||||
| chr11:63245075-63245354 | Common:1; Rare:42 | ||||
| chr11:63644176-63644373 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:63698155-63698355 | Common:1; Rare:36 |