| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65355109-65355734 | Common:7; Rare:244 | ||||
| chr11:65381807-65382231 | Common:8; Rare:192 | ||||
| chr11:65382337-65382970 | Common:10; Rare:226 | ||||
| chr11:65386394-65386764 | Common:2; Rare:247 | ||||
| chr11:65524760-65525219 | Rare:164 | ||||
| chr11:65525180-65525750 | Rare:205 | ||||
| chr11:65539770-65540110 | Common:6; Rare:315; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr11:65540100-65540305 | Rare:153 | ||||
| chr11:65540300-65540520 | Common:2; Rare:101 | ||||
| chr11:65540551-65540830 | Common:11; Rare:280 | ||||
| chr11:65541718-65542256 | Common:4; Rare:148 | ||||
| chr11:65546473-65547101 | Common:8; Rare:370; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr11:65551213-65551367 | Common:1; Rare:41 | ||||
| chr11:65553208-65553784 | Common:7; Rare:294; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:65557950-65558910 | Common:14; Rare:349 |