| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47426146-47426277 | Rare:51 | ||||
| chr11:47426412-47426671 | Rare:61 | ||||
| chr11:47553030-47553361 | Common:2; Rare:116 | ||||
| chr11:47565493-47565804 | Common:4; Rare:74 | ||||
| chr11:47578654-47579136 | Common:1; Rare:172; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642452-47642723 | Rare:108 | ||||
| chr11:47848311-47848406 | Rare:51 | ||||
| chr11:57181743-57182009 | Common:1; Rare:87 | ||||
| chr11:57335738-57335953 | Common:4; Rare:49 | ||||
| chr11:57427085-57427186 | Common:1; Rare:30 | ||||
| chr11:57530693-57531029 | Common:1; Rare:85 | ||||
| chr11:57567605-57567992 | Common:2; Rare:102 | ||||
| chr11:57657522-57657794 | Common:4; Rare:68 | ||||
| chr11:57711972-57712084 | Common:1; Rare:41 | ||||
| chr11:57712153-57712630 | Common:9; Rare:160 |