| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39437297-39437456 | Common:2; Rare:57 | ||||
| chr2:42169209-42169429 | Common:1; Rare:121 | ||||
| chr2:42792543-42792849 | Common:3; Rare:89 | ||||
| chr2:43595978-43596138 | Common:1; Rare:48 | ||||
| chr2:44361483-44362005 | Common:3; Rare:165 | ||||
| chr2:46617019-46617262 | Common:7; Rare:106 | ||||
| chr2:46699019-46699334 | Common:1; Rare:93 | ||||
| chr2:46915738-46915908 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916033-46916161 | Common:2; Rare:43 | ||||
| chr2:47176456-47176858 | Common:4; Rare:179; Clinvar (benign):4 | ||||
| chr2:47402951-47403189 | Common:1; Rare:107; Clinvar:32; Clinvar (benign):26 | ||||
| chr2:47905507-47905847 | Common:3; Rare:169 | ||||
| chr2:48314381-48314744 | Rare:132 | ||||
| chr2:48440619-48440821 | Common:6; Rare:85 | ||||
| chr2:53767559-53767866 | Common:4; Rare:106 |