| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119317097-119317275 | Rare:59 | ||||
| chr11:123062430-123062639 | Common:3; Rare:89 | ||||
| chr11:124673720-124673920 | Common:4; Rare:57 | ||||
| chr11:125164558-125164762 | Rare:37 | ||||
| chr11:125903188-125903328 | Rare:32 | ||||
| chr11:126211641-126211804 | Rare:75 | ||||
| chr11:126268829-126269160 | Common:1; Rare:120; Clinvar:1 | ||||
| chr11:126303979-126304105 | Rare:74 | ||||
| chr11:130448430-130448650 | Rare:52 | ||||
| chr11:130916437-130916505 | Common:2; Rare:28 | ||||
| chr11:134253301-134253586 | Common:2; Rare:93; Clinvar (benign):1 | ||||
| chr11:134331689-134332023 | Common:10; Rare:74 | ||||
| chr12:389249-389383 | Rare:51 | ||||
| chr12:401434-401655 | Common:1; Rare:60 | ||||
| chr12:2004439-2004631 | Common:1; Rare:64 |