| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:231337803-231338056 | Common:2; Rare:92 | ||||
| chr1:231528482-231528820 | Common:2; Rare:111 | ||||
| chr1:232950488-232950682 | Common:3; Rare:62 | ||||
| chr1:233613497-233613671 | Common:1; Rare:46 | ||||
| chr1:233613918-233614166 | Common:5; Rare:75 | ||||
| chr1:234373311-234373800 | Common:1; Rare:215; Clinvar (benign):7 | ||||
| chr1:234607912-234608337 | Common:4; Rare:141 | ||||
| chr1:235128708-235129025 | Rare:132 | ||||
| chr1:235161067-235161304 | Common:2; Rare:123 | ||||
| chr1:235328037-235328616 | Common:4; Rare:171 | ||||
| chr1:235504420-235504740 | Common:4; Rare:96 | ||||
| chr1:235866842-235867125 | Common:3; Rare:80 | ||||
| chr1:235883650-235883880 | Rare:44 | ||||
| chr1:236064922-236064963 | Rare:11 | ||||
| chr1:236064991-236065367 | Common:3; Rare:135; Clinvar (pathogenic):1 |