| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:36597876-36598227 | Common:20; Rare:160 | ||||
| chr2:36966586-36966834 | Common:3; Rare:105 | ||||
| chr2:37084262-37084597 | Common:5; Rare:124 | ||||
| chr2:37196438-37196531 | Rare:37 | ||||
| chr2:37231487-37231887 | Common:6; Rare:197; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:37231889-37232117 | Common:2; Rare:61 | ||||
| chr2:37324731-37325134 | Common:1; Rare:137 | ||||
| chr2:37344408-37344726 | Common:2; Rare:95 | ||||
| chr2:37671506-37671846 | Common:11; Rare:134 | ||||
| chr2:37672163-37672526 | Common:9; Rare:96 | ||||
| chr2:37925457-37925559 | Rare:41 | ||||
| chr2:37950349-37950520 | Common:2; Rare:50 | ||||
| chr2:38076149-38076291 | Rare:38 | ||||
| chr2:38602895-38603163 | Common:4; Rare:106 | ||||
| chr2:38666021-38666152 | Common:1; Rare:41 |