| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47578959-47579113 | Rare:80; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642458-47642713 | Rare:101 | ||||
| chr11:47848291-47848658 | Common:4; Rare:136 | ||||
| chr11:57427075-57427236 | Common:1; Rare:49 | ||||
| chr11:57712175-57712621 | Common:9; Rare:148 | ||||
| chr11:57741259-57741609 | Common:1; Rare:133 | ||||
| chr11:59142681-59142945 | Common:1; Rare:48 | ||||
| chr11:60906427-60906651 | Rare:57 | ||||
| chr11:60913835-60914244 | Common:1; Rare:87 | ||||
| chr11:60952266-60952422 | Rare:38 | ||||
| chr11:61333028-61333266 | Rare:83 | ||||
| chr11:61361842-61362029 | Common:1; Rare:44 | ||||
| chr11:61362267-61362413 | Common:1; Rare:41; Clinvar:6 | ||||
| chr11:61392527-61392652 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429920-61430170 | Common:1; Rare:115; Clinvar:3; Clinvar (benign):5 |