| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:228457847-228458118 | Common:1; Rare:98 | ||||
| chr1:229271003-229271366 | Rare:115 | ||||
| chr1:229434002-229434214 | Common:3; Rare:52; Clinvar (benign):2 | ||||
| chr1:229508215-229508474 | Common:1; Rare:102 | ||||
| chr1:229625938-229626277 | Rare:111 | ||||
| chr1:230642358-230642574 | Common:1; Rare:84 | ||||
| chr1:230978769-230979127 | Common:2; Rare:138 | ||||
| chr1:231241104-231241367 | Common:2; Rare:130; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:231337823-231338056 | Common:2; Rare:84 | ||||
| chr1:231528515-231528738 | Common:2; Rare:79 | ||||
| chr1:232805311-232805446 | Common:2; Rare:75 | ||||
| chr1:232950398-232950664 | Common:4; Rare:98 | ||||
| chr1:234373298-234373582 | Common:1; Rare:130; Clinvar (benign):4 | ||||
| chr1:234373586-234373775 | Rare:77; Clinvar (benign):3 | ||||
| chr1:234608014-234608283 | Common:1; Rare:86 |