| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:111122449-111122715 | Common:3; Rare:114 | ||||
| chr2:111884075-111884283 | Common:2; Rare:61 | ||||
| chr2:112254979-112255195 | Common:2; Rare:89 | ||||
| chr2:112275388-112275663 | Common:1; Rare:97 | ||||
| chr2:112275836-112276011 | Rare:44 | ||||
| chr2:112542126-112542504 | Common:2; Rare:118 | ||||
| chr2:112584378-112584674 | Common:1; Rare:88 | ||||
| chr2:112645707-112646056 | Common:1; Rare:128 | ||||
| chr2:112646253-112646445 | Common:1; Rare:68 | ||||
| chr2:112764594-112764859 | Common:2; Rare:87; Clinvar (pathogenic):1 | ||||
| chr2:113437551-113437924 | Common:4; Rare:132 | ||||
| chr2:113627009-113627329 | Common:4; Rare:95 | ||||
| chr2:113756556-113756791 | Common:3; Rare:82 | ||||
| chr2:113889693-113890290 | Common:9; Rare:190 | ||||
| chr2:118014033-118014275 | Common:3; Rare:128 |