| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219543011-219543442 | Common:8; Rare:353 | ||||
| chr2:219543500-219544143 | Common:21; Rare:933 | ||||
| chr2:219552240-219552944 | Common:11; Rare:815; Clinvar:4; Clinvar (benign):7 | ||||
| chr2:219570901-219571301 | Common:8; Rare:158; Clinvar:7; Clinvar (benign):7 | ||||
| chr2:219571370-219572317 | Common:63; Rare:777; Clinvar:15 | ||||
| chr2:219597604-219597909 | Common:7; Rare:537 | ||||
| chr2:219597861-219598315 | Common:8; Rare:630 | ||||
| chr2:222655890-222656608 | Common:19; Rare:907 | ||||
| chr2:222860720-222861126 | Common:12; Rare:631 | ||||
| chr2:223051952-223052352 | Common:1; Rare:87 | ||||
| chr2:223837490-223838220 | Common:6; Rare:291 | ||||
| chr2:223945200-223945530 | Common:1; Rare:213 | ||||
| chr2:223957177-223957577 | Common:23; Rare:606; Clinvar (benign):2 | ||||
| chr2:224031394-224031857 | Common:59; Rare:988 | ||||
| chr2:224401315-224401724 | Rare:222 |