| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46542273-46542287 | Rare:2 | ||||
| chr2:46616978-46617270 | Common:7; Rare:129 | ||||
| chr2:46698944-46699340 | Common:1; Rare:120 | ||||
| chr2:46915714-46915929 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916032-46916167 | Common:2; Rare:46 | ||||
| chr2:46941652-46941785 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:47034066-47034215 | Common:1; Rare:36 | ||||
| chr2:47176410-47176902 | Common:4; Rare:224; Clinvar (benign):5 | ||||
| chr2:47345052-47345198 | Rare:44 | ||||
| chr2:47402903-47403189 | Common:1; Rare:127; Clinvar:39; Clinvar (benign):27 | ||||
| chr2:47782959-47783189 | Common:2; Rare:101; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:47813813-47814073 | Rare:65 | ||||
| chr2:47905489-47905848 | Common:3; Rare:177 | ||||
| chr2:47906126-47906265 | Rare:47 | ||||
| chr2:48314196-48315064 | Common:2; Rare:322 |