| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:226739279-226739413 | Common:4; Rare:30 | ||||
| chr1:226870517-226870638 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr1:226939947-226940340 | Rare:135; Clinvar:3 | ||||
| chr1:227735208-227735498 | Common:5; Rare:168 | ||||
| chr1:228082456-228082763 | Common:4; Rare:123 | ||||
| chr1:228103239-228103517 | Common:1; Rare:103 | ||||
| chr1:228109223-228109486 | Rare:89 | ||||
| chr1:228139848-228140087 | Common:1; Rare:58 | ||||
| chr1:229271027-229271280 | Rare:88 | ||||
| chr1:229508278-229508474 | Common:1; Rare:78 | ||||
| chr1:229625672-229625864 | Rare:39 | ||||
| chr1:229625964-229626270 | Rare:103 | ||||
| chr1:231241107-231241362 | Common:2; Rare:126; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:231337839-231338319 | Common:4; Rare:142 | ||||
| chr1:231528490-231528741 | Common:2; Rare:85 |