| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:228457866-228458114 | Common:1; Rare:79 | ||||
| chr1:229271036-229271303 | Rare:90 | ||||
| chr1:229508275-229508489 | Common:1; Rare:88 | ||||
| chr1:229625964-229626254 | Rare:94 | ||||
| chr1:231241110-231241358 | Common:2; Rare:119; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:231337839-231338061 | Common:2; Rare:75 | ||||
| chr1:231528540-231528733 | Common:2; Rare:72 | ||||
| chr1:232950497-232950640 | Common:1; Rare:49 | ||||
| chr1:234373373-234373601 | Common:1; Rare:115; Clinvar (benign):4 | ||||
| chr1:234373642-234373768 | Rare:51; Clinvar (benign):3 | ||||
| chr1:235866883-235867139 | Common:2; Rare:76 | ||||
| chr1:236604466-236604657 | Common:4; Rare:55 | ||||
| chr1:241519676-241519982 | Common:2; Rare:94; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr1:241848129-241848282 | Common:1; Rare:22 | ||||
| chr1:243255201-243255442 | Common:1; Rare:58 |