| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:212791712-212791990 | Common:6; Rare:133 | ||||
| chr1:212858080-212858318 | Common:4; Rare:62; Clinvar:2 | ||||
| chr1:212950357-212950609 | Common:2; Rare:61 | ||||
| chr1:213015217-213015633 | Rare:108 | ||||
| chr1:213015658-213015951 | Rare:90 | ||||
| chr1:213050952-213051351 | Common:3; Rare:99 | ||||
| chr1:214280930-214281310 | Common:3; Rare:155 | ||||
| chr1:214281402-214281630 | Common:3; Rare:113 | ||||
| chr1:214551548-214551948 | Common:2; Rare:126 | ||||
| chr1:214552285-214552599 | Common:4; Rare:57 | ||||
| chr1:214602903-214603284 | Common:3; Rare:108 | ||||
| chr1:215567052-215567422 | Common:2; Rare:100 | ||||
| chr1:217631015-217631398 | Common:3; Rare:115 | ||||
| chr1:218285154-218285388 | Common:4; Rare:106 | ||||
| chr1:218345955-218346092 | Common:5; Rare:46; Clinvar:7; Clinvar (benign):3 |