| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10448488-10448713 | Rare:75 | ||||
| chr2:10689892-10690038 | Common:2; Rare:53 | ||||
| chr2:10812683-10812984 | Common:3; Rare:115 | ||||
| chr2:11466063-11466325 | Common:5; Rare:71 | ||||
| chr2:11482624-11482938 | Common:2; Rare:97 | ||||
| chr2:11746364-11746671 | Common:2; Rare:86; Clinvar:4 | ||||
| chr2:12716748-12717075 | Common:1; Rare:92 | ||||
| chr2:12718177-12718244 | Common:1; Rare:13 | ||||
| chr2:15561294-15561415 | Rare:48 | ||||
| chr2:15940351-15940564 | Rare:52 | ||||
| chr2:17518336-17518635 | Common:3; Rare:108 | ||||
| chr2:17540443-17540714 | Common:1; Rare:65 | ||||
| chr2:17753689-17754174 | Common:5; Rare:149; Clinvar (benign):1 | ||||
| chr2:18560279-18560474 | Rare:82 | ||||
| chr2:18560643-18560808 | Rare:48 |