| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:111122427-111122744 | Common:3; Rare:133 | ||||
| chr2:111884075-111884266 | Common:1; Rare:55 | ||||
| chr2:111898305-111898625 | Common:2; Rare:70 | ||||
| chr2:112254998-112255182 | Common:2; Rare:81 | ||||
| chr2:112275356-112275634 | Common:1; Rare:100 | ||||
| chr2:112481938-112482286 | Common:2; Rare:122 | ||||
| chr2:112542088-112542493 | Common:1; Rare:130 | ||||
| chr2:112584346-112584637 | Common:1; Rare:80 | ||||
| chr2:112584772-112584895 | Rare:27 | ||||
| chr2:112645715-112645944 | Common:1; Rare:84 | ||||
| chr2:112646261-112646445 | Common:1; Rare:65 | ||||
| chr2:112764569-112764984 | Common:5; Rare:150; Clinvar (pathogenic):1 | ||||
| chr2:113437615-113437924 | Common:4; Rare:123 | ||||
| chr2:113627041-113627289 | Common:2; Rare:75 | ||||
| chr2:113756576-113756799 | Common:3; Rare:83 |