| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:232950429-232950656 | Common:4; Rare:87 | ||||
| chr1:233295060-233295255 | Common:2; Rare:49 | ||||
| chr1:233295707-233295833 | Common:1; Rare:36 | ||||
| chr1:233327464-233327803 | Common:5; Rare:55 | ||||
| chr1:233613462-233613584 | Rare:24 | ||||
| chr1:233613718-233614008 | Rare:66 | ||||
| chr1:233614277-233614379 | Rare:39 | ||||
| chr1:233904530-233904761 | Common:3; Rare:68 | ||||
| chr1:234373235-234373570 | Common:1; Rare:142; Clinvar (benign):4 | ||||
| chr1:234373645-234373771 | Rare:49; Clinvar (benign):3 | ||||
| chr1:234478930-234479238 | Common:6; Rare:132 | ||||
| chr1:234608059-234608459 | Common:2; Rare:218 | ||||
| chr1:234609492-234609629 | Common:1; Rare:85 | ||||
| chr1:235128792-235129106 | Common:1; Rare:119 | ||||
| chr1:235161186-235161419 | Common:1; Rare:151 |