| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:235328104-235328639 | Common:8; Rare:281 | ||||
| chr1:235328660-235329000 | Common:2; Rare:170 | ||||
| chr1:235504371-235504788 | Common:10; Rare:260 | ||||
| chr1:235504910-235505240 | Common:1; Rare:118 | ||||
| chr1:235649919-235650361 | Common:10; Rare:206 | ||||
| chr1:236065062-236065342 | Common:2; Rare:110; Clinvar (pathogenic):1 | ||||
| chr1:236281929-236282258 | Common:12; Rare:185 | ||||
| chr1:236523216-236524045 | Common:14; Rare:328 | ||||
| chr1:236524437-236524651 | Common:4; Rare:101 | ||||
| chr1:236604427-236604626 | Common:8; Rare:117 | ||||
| chr1:236794951-236795545 | Common:14; Rare:398; Clinvar:11; Clinvar (benign):2 | ||||
| chr1:241519671-241519982 | Common:4; Rare:188; Clinvar:21; Clinvar (benign):13; Clinvar (pathogenic):6 | ||||
| chr1:241640244-241640568 | Common:14; Rare:206 | ||||
| chr1:241848078-241848275 | Common:4; Rare:69 | ||||
| chr1:243255035-243255395 | Common:2; Rare:128 |