| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119368432-119368563 | Rare:40 | ||||
| chr11:126367110-126367388 | Common:2; Rare:56 | ||||
| chr11:126384643-126384847 | Common:1; Rare:34 | ||||
| chr11:129817338-129817454 | Common:3; Rare:23 | ||||
| chr11:129817789-129818061 | Rare:40 | ||||
| chr11:130146510-130146646 | Common:1; Rare:18 | ||||
| chr11:130200100-130200267 | Rare:46 | ||||
| chr11:134467018-134467320 | Rare:47 | ||||
| chr12:16769-16843 | Common:4; Rare:25 | ||||
| chr12:508944-509046 | Common:1; Rare:13 | ||||
| chr12:521581-521858 | Common:5; Rare:60 | ||||
| chr12:546666-546977 | Common:4; Rare:61 | ||||
| chr12:753872-754183 | Common:1; Rare:123; Clinvar:7; Clinvar (benign):3 | ||||
| chr12:917334-917475 | Rare:26 | ||||
| chr12:1581743-1582137 | Rare:76 |