| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:111884108-111884283 | Common:1; Rare:54 | ||||
| chr2:111898298-111898686 | Common:2; Rare:84 | ||||
| chr2:112055538-112055612 | Common:1; Rare:26 | ||||
| chr2:112275388-112275642 | Common:1; Rare:89 | ||||
| chr2:112542105-112542493 | Common:1; Rare:121 | ||||
| chr2:112584346-112584633 | Common:1; Rare:79 | ||||
| chr2:112584785-112584854 | Rare:17 | ||||
| chr2:112645701-112645968 | Common:1; Rare:103 | ||||
| chr2:112764594-112764836 | Common:2; Rare:75; Clinvar (pathogenic):1 | ||||
| chr2:113127378-113127657 | Rare:63; Clinvar (benign):1 | ||||
| chr2:113437592-113437913 | Common:4; Rare:119 | ||||
| chr2:113627041-113627330 | Common:4; Rare:83 | ||||
| chr2:113756507-113756791 | Common:4; Rare:96 | ||||
| chr2:113889694-113890290 | Common:9; Rare:190 | ||||
| chr2:113890925-113891271 | Rare:68 |