| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10689925-10690094 | Common:5; Rare:55 | ||||
| chr2:10812683-10812971 | Common:3; Rare:113 | ||||
| chr2:11746505-11746671 | Common:2; Rare:55; Clinvar:4 | ||||
| chr2:12716589-12717069 | Common:4; Rare:155 | ||||
| chr2:15561279-15561390 | Rare:52 | ||||
| chr2:17753721-17754168 | Common:4; Rare:142; Clinvar (benign):1 | ||||
| chr2:19358557-19358782 | Rare:50 | ||||
| chr2:19901634-19901792 | Common:1; Rare:89 | ||||
| chr2:19901937-19902131 | Common:3; Rare:60 | ||||
| chr2:19990039-19990252 | Rare:61 | ||||
| chr2:20051481-20051841 | Common:1; Rare:104 | ||||
| chr2:20350828-20351060 | Common:1; Rare:96 | ||||
| chr2:20446841-20447074 | Common:3; Rare:93 | ||||
| chr2:20651037-20651276 | Rare:75 | ||||
| chr2:20823056-20823159 | Rare:41 |