| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112255011-112255175 | Common:1; Rare:76 | ||||
| chr2:112275394-112275594 | Common:1; Rare:64 | ||||
| chr2:112542094-112542504 | Common:2; Rare:133 | ||||
| chr2:112584382-112584645 | Common:1; Rare:73 | ||||
| chr2:112584770-112584859 | Rare:21 | ||||
| chr2:112645605-112645972 | Common:2; Rare:130 | ||||
| chr2:112764115-112764251 | Common:1; Rare:43 | ||||
| chr2:112764572-112764859 | Common:2; Rare:98; Clinvar (pathogenic):1 | ||||
| chr2:112764872-112764970 | Common:2; Rare:45 | ||||
| chr2:112784459-112784563 | Rare:22 | ||||
| chr2:112836755-112837108 | Common:1; Rare:53; Clinvar:1 | ||||
| chr2:113627041-113627303 | Common:3; Rare:78 | ||||
| chr2:113756507-113756781 | Common:4; Rare:90 | ||||
| chr2:113889709-113890314 | Common:9; Rare:191 | ||||
| chr2:113891001-113891151 | Rare:34 |