| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:232950479-232950664 | Common:3; Rare:64 | ||||
| chr1:233613918-233614190 | Common:5; Rare:81 | ||||
| chr1:234373302-234373554 | Common:1; Rare:121; Clinvar (benign):3 | ||||
| chr1:235327771-235328073 | Rare:86 | ||||
| chr1:235328479-235328579 | Common:1; Rare:29 | ||||
| chr1:235504420-235504732 | Common:4; Rare:94 | ||||
| chr1:235866858-235867125 | Common:3; Rare:79 | ||||
| chr1:236064991-236065417 | Common:4; Rare:142; Clinvar (pathogenic):1 | ||||
| chr1:236523876-236524025 | Common:2; Rare:38 | ||||
| chr1:236524532-236524608 | Common:1; Rare:13 | ||||
| chr1:236795642-236795704 | Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:239719073-239719220 | Common:1; Rare:24 | ||||
| chr1:241848121-241848248 | Common:1; Rare:24 | ||||
| chr1:243255783-243256163 | Common:1; Rare:113; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:244451752-244452078 | Rare:113 |