| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200306250-200306560 | Common:5; Rare:76 | ||||
| chr2:200889054-200889385 | Common:2; Rare:108 | ||||
| chr2:201071620-201072012 | Rare:79 | ||||
| chr2:201451542-201451866 | Common:3; Rare:83 | ||||
| chr2:201642637-201642727 | Rare:45 | ||||
| chr2:201643457-201643553 | Rare:27; Clinvar:3 | ||||
| chr2:201780896-201780979 | Common:2; Rare:24; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:202265625-202265791 | Rare:56 | ||||
| chr2:202912125-202912291 | Common:2; Rare:56 | ||||
| chr2:206086141-206086275 | Rare:15 | ||||
| chr2:206159396-206159672 | Common:2; Rare:92 | ||||
| chr2:206765324-206765615 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:207529695-207530001 | Common:3; Rare:97 | ||||
| chr2:208255069-208255214 | Common:2; Rare:39 | ||||
| chr2:208266019-208266298 | Common:9; Rare:97; Clinvar:1; Clinvar (benign):2 |