| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207165929-207166383 | Common:3; Rare:141 | ||||
| chr2:207166827-207167117 | Common:4; Rare:115 | ||||
| chr2:207529970-207530119 | Rare:33 | ||||
| chr2:207625256-207625619 | Common:1; Rare:102 | ||||
| chr2:208025519-208025724 | Common:2; Rare:49 | ||||
| chr2:208255069-208255239 | Common:2; Rare:47 | ||||
| chr2:208266119-208266409 | Common:6; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002420-210002643 | Common:3; Rare:76 | ||||
| chr2:210171215-210171543 | Common:4; Rare:124 | ||||
| chr2:213284210-213284480 | Rare:85 | ||||
| chr2:214809680-214809995 | Common:1; Rare:115; Clinvar:1 | ||||
| chr2:215311932-215312119 | Common:5; Rare:78 | ||||
| chr2:216081777-216081916 | Common:1; Rare:49 | ||||
| chr2:216498744-216498890 | Common:4; Rare:62 | ||||
| chr2:218216947-218217356 | Common:3; Rare:131 |