| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201260546-201260946 | Rare:67 | ||||
| chr2:201433410-201433884 | Common:11; Rare:200 | ||||
| chr2:201451408-201451860 | Common:7; Rare:602 | ||||
| chr2:201642330-201642840 | Common:10; Rare:618; Clinvar (benign):4 | ||||
| chr2:201643015-201643415 | Common:11; Rare:153; Clinvar (benign):2 | ||||
| chr2:201780620-201780830 | Common:2; Rare:54 | ||||
| chr2:201780868-201781457 | Common:16; Rare:666; Clinvar:15; Clinvar (benign):12 | ||||
| chr2:202033954-202034354 | Common:2; Rare:152 | ||||
| chr2:202221834-202222234 | Common:8; Rare:123 | ||||
| chr2:202238220-202238430 | Rare:58 | ||||
| chr2:202238512-202239097 | Common:2; Rare:326 | ||||
| chr2:202265522-202265922 | Common:2; Rare:512 | ||||
| chr2:202375813-202376970 | Common:7; Rare:542; Clinvar:10; Clinvar (benign):9 | ||||
| chr2:202376994-202378194 | Common:6; Rare:748; Clinvar:6; Clinvar (benign):14; Clinvar (pathogenic):7 | ||||
| chr2:202634658-202635128 | Common:29; Rare:649 |