| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37156915-37157046 | Common:1; Rare:43 | ||||
| chr2:37231551-37231726 | Common:4; Rare:102; Clinvar (benign):4 | ||||
| chr2:37324731-37324931 | Common:1; Rare:84 | ||||
| chr2:37344479-37344734 | Common:2; Rare:84 | ||||
| chr2:37925219-37925354 | Rare:53 | ||||
| chr2:38076132-38076291 | Rare:40 | ||||
| chr2:38751349-38751595 | Common:3; Rare:107 | ||||
| chr2:38875897-38876059 | Common:1; Rare:57 | ||||
| chr2:39437100-39437464 | Common:4; Rare:128 | ||||
| chr2:42169160-42169436 | Common:1; Rare:135 | ||||
| chr2:43595937-43596222 | Common:1; Rare:103 | ||||
| chr2:43676362-43676496 | Common:2; Rare:35 | ||||
| chr2:44361479-44362002 | Common:3; Rare:164 | ||||
| chr2:46616982-46617270 | Common:7; Rare:128 | ||||
| chr2:46699080-46699440 | Common:2; Rare:106 |