| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:229271022-229271322 | Rare:98 | ||||
| chr1:229508253-229508453 | Common:1; Rare:81 | ||||
| chr1:229625950-229626261 | Rare:100 | ||||
| chr1:230978753-230979102 | Common:2; Rare:134 | ||||
| chr1:231241107-231241262 | Rare:87; Clinvar:3 | ||||
| chr1:231337830-231338088 | Common:3; Rare:89 | ||||
| chr1:231528537-231528750 | Common:2; Rare:77 | ||||
| chr1:234373339-234373539 | Common:1; Rare:101; Clinvar (benign):3 | ||||
| chr1:234373636-234373788 | Rare:55; Clinvar (benign):3 | ||||
| chr1:234608071-234608289 | Common:1; Rare:70 | ||||
| chr1:235327900-235328073 | Rare:47 | ||||
| chr1:235866852-235867177 | Common:3; Rare:102 | ||||
| chr1:236064991-236065356 | Common:3; Rare:132; Clinvar (pathogenic):1 | ||||
| chr1:236523846-236524034 | Common:2; Rare:51 | ||||
| chr1:236795109-236795453 | Common:5; Rare:145; Clinvar:3 |