| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:233327453-233327786 | Common:5; Rare:51 | ||||
| chr1:234214199-234214293 | Rare:14 | ||||
| chr1:234373029-234373183 | Common:3; Rare:34 | ||||
| chr1:234373225-234373590 | Common:1; Rare:152; Clinvar (benign):4 | ||||
| chr1:234373608-234373788 | Rare:71; Clinvar (benign):3 | ||||
| chr1:234373884-234374016 | Rare:28 | ||||
| chr1:234478610-234478750 | Common:2; Rare:41 | ||||
| chr1:234479062-234479240 | Common:5; Rare:73 | ||||
| chr1:234609308-234609438 | Common:1; Rare:33 | ||||
| chr1:234609490-234609704 | Common:1; Rare:126 | ||||
| chr1:234609899-234610000 | Rare:36 | ||||
| chr1:235128163-235128497 | Common:3; Rare:81 | ||||
| chr1:235128713-235129135 | Common:1; Rare:172 | ||||
| chr1:235160689-235160941 | Common:3; Rare:73 | ||||
| chr1:235160965-235161024 | Common:1; Rare:16 |