| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:33472290-33472690 | Common:2; Rare:154 | ||||
| chr1:34754766-34755077 | Rare:53 | ||||
| chr1:34781115-34781453 | Common:2; Rare:152; Clinvar:2; Clinvar (benign):4 | ||||
| chr1:34781635-34782035 | Common:2; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:34859668-34859921 | Common:2; Rare:119 | ||||
| chr1:34984750-34985090 | Common:3; Rare:153 | ||||
| chr1:34985278-34985380 | Common:1; Rare:39 | ||||
| chr1:35031620-35032270 | Common:4; Rare:243 | ||||
| chr1:35079315-35079542 | Common:6; Rare:83 | ||||
| chr1:35192220-35192820 | Common:12; Rare:378 | ||||
| chr1:35192860-35193040 | Common:3; Rare:85 | ||||
| chr1:35193051-35193440 | Common:4; Rare:232 | ||||
| chr1:35268618-35269044 | Rare:206 | ||||
| chr1:35557353-35557460 | Rare:29 | ||||
| chr1:35557609-35557866 | Common:4; Rare:192 |