| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:229625962-229626261 | Rare:97 | ||||
| chr1:230978758-230979157 | Common:2; Rare:156 | ||||
| chr1:231241110-231241367 | Common:2; Rare:125; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:231337836-231338056 | Common:2; Rare:76 | ||||
| chr1:231528494-231528738 | Common:2; Rare:82 | ||||
| chr1:232950494-232950669 | Common:2; Rare:60 | ||||
| chr1:234373391-234373775 | Common:1; Rare:175; Clinvar (benign):7 | ||||
| chr1:235328149-235328376 | Common:2; Rare:66 | ||||
| chr1:236281956-236282216 | Common:6; Rare:71 | ||||
| chr1:236523814-236524024 | Common:3; Rare:57 | ||||
| chr1:236604464-236604611 | Common:4; Rare:45 | ||||
| chr1:236795076-236795323 | Common:5; Rare:86; Clinvar:1 | ||||
| chr1:241848114-241848236 | Common:1; Rare:23 | ||||
| chr1:243255040-243255420 | Common:1; Rare:89 | ||||
| chr1:243255776-243256157 | Common:1; Rare:114; Clinvar:4; Clinvar (benign):1 |