| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9843227-9843539 | Common:6; Rare:95 | ||||
| chr2:10123146-10123250 | Rare:22 | ||||
| chr2:10689910-10690002 | Common:2; Rare:32 | ||||
| chr2:11465857-11466184 | Common:3; Rare:101 | ||||
| chr2:11539484-11539738 | Rare:39 | ||||
| chr2:11746489-11746655 | Common:1; Rare:50; Clinvar:2 | ||||
| chr2:12716629-12717062 | Common:3; Rare:132 | ||||
| chr2:15591378-15591692 | Common:2; Rare:51 | ||||
| chr2:17540416-17540745 | Common:1; Rare:81 | ||||
| chr2:17753689-17754174 | Common:5; Rare:149; Clinvar (benign):1 | ||||
| chr2:18560663-18560808 | Rare:38 | ||||
| chr2:19901628-19901741 | Common:1; Rare:58 | ||||
| chr2:19901905-19902048 | Common:1; Rare:43 | ||||
| chr2:19990043-19990211 | Rare:45 | ||||
| chr2:20225116-20225262 | Common:1; Rare:33 |