| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126211641-126211809 | Rare:77 | ||||
| chr11:126268835-126269191 | Common:1; Rare:132; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:126303979-126304081 | Rare:58 | ||||
| chr11:126355534-126355742 | Common:1; Rare:53 | ||||
| chr11:128522257-128522518 | Common:1; Rare:80 | ||||
| chr11:129895535-129895666 | Common:2; Rare:48 | ||||
| chr11:130069653-130069980 | Common:2; Rare:118 | ||||
| chr11:131911346-131911484 | Common:1; Rare:55 | ||||
| chr11:134253301-134253586 | Common:2; Rare:93; Clinvar (benign):1 | ||||
| chr12:389249-389357 | Rare:39 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:991109-991254 | Common:1; Rare:54 | ||||
| chr12:2004435-2004669 | Common:2; Rare:69 | ||||
| chr12:2877009-2877272 | Rare:83 | ||||
| chr12:3077246-3077428 | Common:6; Rare:78 |