| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:313721-314344 | Common:2; Rare:156 | ||||
| chr11:314799-315092 | Common:3; Rare:85 | ||||
| chr11:320558-320924 | Common:5; Rare:144; Clinvar:1 | ||||
| chr11:407097-407423 | Common:9; Rare:103 | ||||
| chr11:498803-499036 | Common:2; Rare:113 | ||||
| chr11:504446-504743 | Common:3; Rare:79 | ||||
| chr11:506751-506994 | Common:2; Rare:79 | ||||
| chr11:576412-576538 | Rare:52 | ||||
| chr11:615936-616027 | Rare:27 | ||||
| chr11:695772-695817 | Rare:19 | ||||
| chr11:706511-706668 | Rare:30 | ||||
| chr11:707061-707086 | Rare:4 | ||||
| chr11:747323-747507 | Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:764198-764412 | Rare:71; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:777463-777598 | Common:1; Rare:59 |