| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208253994-208254540 | Common:3; Rare:225 | ||||
| chr2:208254939-208255272 | Common:4; Rare:160 | ||||
| chr2:208266026-208266418 | Common:17; Rare:258; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:210002439-210002782 | Common:11; Rare:197 | ||||
| chr2:210170630-210171010 | Common:4; Rare:241 | ||||
| chr2:210171269-210171569 | Common:8; Rare:189 | ||||
| chr2:210476629-210476843 | Common:2; Rare:67 | ||||
| chr2:210477534-210477720 | Rare:103 | ||||
| chr2:213151542-213152034 | Common:4; Rare:312 | ||||
| chr2:213284198-213284500 | Rare:192 | ||||
| chr2:214809501-214810376 | Common:47; Rare:996; Clinvar:17; Clinvar (benign):18 | ||||
| chr2:215311871-215312180 | Common:15; Rare:204 | ||||
| chr2:215435640-215436160 | Common:6; Rare:257 | ||||
| chr2:216013269-216013395 | Common:1; Rare:46 | ||||
| chr2:216081676-216081952 | Common:2; Rare:162 |