| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67277093-67277238 | Rare:34 | ||||
| chr11:67277453-67277811 | Common:1; Rare:94 | ||||
| chr11:67317177-67317316 | Common:1; Rare:24 | ||||
| chr11:67344383-67344533 | Rare:23 | ||||
| chr11:67345312-67345533 | Rare:49 | ||||
| chr11:67351194-67351395 | Common:1; Rare:32 | ||||
| chr11:67352179-67352561 | Rare:83 | ||||
| chr11:67354264-67354512 | Rare:38 | ||||
| chr11:67372490-67372777 | Common:2; Rare:75 | ||||
| chr11:67381006-67381216 | Rare:33 | ||||
| chr11:67381346-67381613 | Common:3; Rare:56 | ||||
| chr11:67427550-67427757 | Common:1; Rare:37 | ||||
| chr11:67436295-67436769 | Common:2; Rare:119 | ||||
| chr11:67437044-67437407 | Common:1; Rare:97 | ||||
| chr11:67459604-67459824 | Common:1; Rare:32; Clinvar:2; Clinvar (benign):1 |