| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:231528515-231528758 | Common:2; Rare:84 | ||||
| chr1:232805295-232805444 | Common:2; Rare:84 | ||||
| chr1:232950488-232950664 | Common:3; Rare:59 | ||||
| chr1:234373347-234373775 | Common:1; Rare:197; Clinvar (benign):7 | ||||
| chr1:235128674-235129072 | Common:1; Rare:167 | ||||
| chr1:235327900-235328073 | Rare:47 | ||||
| chr1:235328109-235328681 | Common:5; Rare:172 | ||||
| chr1:235328825-235329051 | Common:1; Rare:71 | ||||
| chr1:235650558-235650656 | Rare:28 | ||||
| chr1:235866852-235867125 | Common:3; Rare:79 | ||||
| chr1:236065066-236065326 | Common:2; Rare:104; Clinvar (pathogenic):1 | ||||
| chr1:236281943-236282219 | Common:6; Rare:74 | ||||
| chr1:236523864-236524060 | Common:2; Rare:50 | ||||
| chr1:236604453-236604573 | Common:4; Rare:38 | ||||
| chr1:236795086-236795436 | Common:5; Rare:146; Clinvar:3 |