| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202377006-202377382 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:202377554-202377690 | Rare:38 | ||||
| chr2:202634721-202635068 | Common:6; Rare:118 | ||||
| chr2:202635834-202636297 | Common:6; Rare:126 | ||||
| chr2:202870683-202870850 | Common:2; Rare:26 | ||||
| chr2:202871344-202871534 | Common:4; Rare:54 | ||||
| chr2:202871623-202871733 | Rare:40 | ||||
| chr2:202871993-202872125 | Rare:29 | ||||
| chr2:202911613-202912024 | Common:1; Rare:84 | ||||
| chr2:202912105-202912295 | Common:2; Rare:64 | ||||
| chr2:202912475-202912584 | Common:2; Rare:36 | ||||
| chr2:203014408-203014949 | Common:1; Rare:162 | ||||
| chr2:203238719-203239447 | Common:3; Rare:250 | ||||
| chr2:203328039-203328445 | Common:2; Rare:149 | ||||
| chr2:203328835-203328994 | Common:1; Rare:50 |