| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9765539-9765691 | Rare:16 | ||||
| chr11:9775607-9775724 | Common:1; Rare:20 | ||||
| chr11:12182731-12183004 | Common:1; Rare:49 | ||||
| chr11:16604273-16604456 | Common:1; Rare:41 | ||||
| chr11:16924981-16925040 | Rare:11 | ||||
| chr11:16925667-16925802 | Rare:36 | ||||
| chr11:17353682-17353775 | Common:4; Rare:30 | ||||
| chr11:19188159-19188553 | Common:4; Rare:112; Clinvar:15; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr11:19209686-19209864 | Common:2; Rare:39 | ||||
| chr11:20044241-20044327 | Rare:26 | ||||
| chr11:20049158-20049247 | Rare:23 | ||||
| chr11:27220077-27220268 | Common:1; Rare:28 | ||||
| chr11:33291424-33291690 | Rare:45 | ||||
| chr11:34692236-34692486 | Common:3; Rare:68 | ||||
| chr11:38424870-38424962 | Rare:21 |