| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43595796-43595839 | Rare:9 | ||||
| chr2:43595863-43596297 | Common:1; Rare:144 | ||||
| chr2:43596352-43596498 | Rare:38 | ||||
| chr2:43637094-43637350 | Common:2; Rare:83 | ||||
| chr2:43676410-43676474 | Rare:17 | ||||
| chr2:43773919-43774127 | Common:5; Rare:82 | ||||
| chr2:43995903-43996487 | Common:6; Rare:260; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:44167762-44168231 | Common:5; Rare:173 | ||||
| chr2:44168258-44168432 | Common:1; Rare:39 | ||||
| chr2:44168530-44169097 | Common:2; Rare:188 | ||||
| chr2:44361385-44361585 | Common:2; Rare:71 | ||||
| chr2:44361746-44362062 | Common:2; Rare:101 | ||||
| chr2:44362241-44362338 | Rare:19 | ||||
| chr2:44362472-44362641 | Common:1; Rare:38 | ||||
| chr2:45009394-45009665 | Common:1; Rare:91 |