| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112254977-112255162 | Common:1; Rare:79 | ||||
| chr2:112275356-112275651 | Common:1; Rare:108 | ||||
| chr2:112275728-112276011 | Rare:69 | ||||
| chr2:112542135-112542493 | Common:1; Rare:112 | ||||
| chr2:112584378-112584647 | Common:1; Rare:74 | ||||
| chr2:112584770-112584854 | Rare:21 | ||||
| chr2:112645707-112645954 | Common:1; Rare:93 | ||||
| chr2:112764561-112764779 | Common:1; Rare:75; Clinvar (pathogenic):1 | ||||
| chr2:112836278-112836292 | Rare:4 | ||||
| chr2:112836774-112836856 | Common:1; Rare:15; Clinvar:1 | ||||
| chr2:113157202-113157517 | Common:3; Rare:83 | ||||
| chr2:113198866-113198983 | Rare:44 | ||||
| chr2:113236936-113236984 | Rare:7 | ||||
| chr2:113627024-113627341 | Common:4; Rare:90 | ||||
| chr2:113756506-113756753 | Common:3; Rare:77 |