| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65314666-65314913 | Rare:76 | ||||
| chr11:65333607-65333908 | Common:1; Rare:127 | ||||
| chr11:65334106-65334192 | Rare:15 | ||||
| chr11:65354517-65354810 | Common:1; Rare:86 | ||||
| chr11:65381787-65382238 | Common:4; Rare:120 | ||||
| chr11:65382548-65382889 | Common:1; Rare:50 | ||||
| chr11:65386365-65386721 | Common:1; Rare:96 | ||||
| chr11:65524784-65525173 | Rare:77 | ||||
| chr11:65540578-65540843 | Common:4; Rare:108 | ||||
| chr11:65540976-65541115 | Common:1; Rare:38 | ||||
| chr11:65546500-65546909 | Common:3; Rare:135; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65552183-65552289 | Common:1; Rare:31 | ||||
| chr11:65558709-65558737 | Rare:3 | ||||
| chr11:65569761-65570133 | Common:2; Rare:121 | ||||
| chr11:65570171-65570539 | Common:2; Rare:130 |