| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:86720732-86720812 | Rare:26 | ||||
| chr2:86721272-86721467 | Common:3; Rare:51 | ||||
| chr2:86747895-86748392 | Common:1; Rare:89 | ||||
| chr2:87825696-87825995 | Rare:100 | ||||
| chr2:88055346-88055575 | Rare:65 | ||||
| chr2:88055666-88055977 | Common:1; Rare:111 | ||||
| chr2:88170248-88170395 | Common:5; Rare:40 | ||||
| chr2:88627381-88627940 | Common:3; Rare:161; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:88691401-88691701 | Common:3; Rare:100 | ||||
| chr2:88691718-88691992 | Rare:100; Clinvar:2 | ||||
| chr2:95121708-95121828 | Common:1; Rare:63 | ||||
| chr2:95121928-95122138 | Rare:63 | ||||
| chr2:95159492-95159856 | Common:4; Rare:107 | ||||
| chr2:95165297-95165565 | Common:1; Rare:60 | ||||
| chr2:95165586-95166014 | Common:1; Rare:117 |