| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126303980-126304081 | Rare:57 | ||||
| chr11:126355542-126355640 | Common:1; Rare:13 | ||||
| chr11:128522132-128522546 | Common:1; Rare:128 | ||||
| chr11:130002790-130002972 | Common:3; Rare:33 | ||||
| chr11:130916403-130916686 | Common:6; Rare:88 | ||||
| chr11:131909710-131909944 | Common:1; Rare:35 | ||||
| chr11:131911121-131911148 | Common:1; Rare:3 | ||||
| chr11:131911171-131911235 | Rare:21 | ||||
| chr11:131911264-131911590 | Common:1; Rare:105 | ||||
| chr11:134253301-134253586 | Common:2; Rare:93; Clinvar (benign):1 | ||||
| chr11:134331689-134332023 | Common:10; Rare:74 | ||||
| chr12:389230-389399 | Common:1; Rare:66 | ||||
| chr12:389491-389644 | Common:5; Rare:70 | ||||
| chr12:401441-401664 | Rare:61 | ||||
| chr12:991114-991342 | Common:4; Rare:98 |