| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:217934761-217934806 | Rare:4 | ||||
| chr2:217940490-217940734 | Rare:52 | ||||
| chr2:217941978-217942335 | Common:3; Rare:66 | ||||
| chr2:217942424-217942506 | Common:1; Rare:17 | ||||
| chr2:218009813-218009888 | Rare:8 | ||||
| chr2:218272359-218272613 | Rare:68 | ||||
| chr2:219418884-219419034 | Rare:46; Clinvar:10; Clinvar (benign):3 | ||||
| chr2:219447460-219447833 | Rare:67 | ||||
| chr2:219453674-219453980 | Common:1; Rare:46 | ||||
| chr2:219462049-219462386 | Rare:84 | ||||
| chr2:223943929-223944140 | Rare:45 | ||||
| chr2:227277266-227277502 | Common:2; Rare:48; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:231199302-231199348 | Rare:8 | ||||
| chr2:231712440-231712888 | Common:4; Rare:136 | ||||
| chr2:240464682-240464882 | Common:3; Rare:80 |