| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37084267-37084563 | Common:4; Rare:111 | ||||
| chr2:37157086-37157370 | Common:7; Rare:61 | ||||
| chr2:37231559-37231696 | Common:4; Rare:75; Clinvar (benign):3 | ||||
| chr2:38377206-38377488 | Common:3; Rare:123 | ||||
| chr2:38751303-38751582 | Common:5; Rare:137 | ||||
| chr2:38875886-38876059 | Common:1; Rare:63 | ||||
| chr2:39437078-39437464 | Common:4; Rare:138 | ||||
| chr2:43595978-43596205 | Common:1; Rare:79 | ||||
| chr2:44361467-44362002 | Common:3; Rare:170 | ||||
| chr2:46617019-46617261 | Common:6; Rare:105 | ||||
| chr2:46698711-46698940 | Common:2; Rare:69 | ||||
| chr2:46915733-46915910 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47345046-47345148 | Rare:26 | ||||
| chr2:47905507-47905645 | Common:3; Rare:81 | ||||
| chr2:48314359-48314783 | Rare:151 |