| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:231818172-231818495 | Common:3; Rare:82; Clinvar:1 | ||||
| chr1:232805209-232805439 | Common:3; Rare:124 | ||||
| chr1:232950488-232950713 | Common:4; Rare:74 | ||||
| chr1:233613462-233613661 | Common:1; Rare:49 | ||||
| chr1:234373274-234373603 | Common:1; Rare:147; Clinvar (benign):4 | ||||
| chr1:234373606-234373839 | Common:1; Rare:93; Clinvar (benign):5 | ||||
| chr1:235128772-235129041 | Rare:107 | ||||
| chr1:235328109-235328627 | Common:4; Rare:159 | ||||
| chr1:235328788-235328967 | Common:1; Rare:65 | ||||
| chr1:235866858-235867177 | Common:3; Rare:102 | ||||
| chr1:236065072-236065356 | Common:3; Rare:109; Clinvar (pathogenic):1 | ||||
| chr1:236604439-236604645 | Common:4; Rare:66 | ||||
| chr1:236686621-236686795 | Common:1; Rare:58; Clinvar:6; Clinvar (benign):7 | ||||
| chr1:236795086-236795453 | Common:5; Rare:153; Clinvar:3 | ||||
| chr1:241519651-241519988 | Common:2; Rare:106; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):4 |