| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:233613916-233614177 | Common:5; Rare:80 | ||||
| chr1:234373326-234373554 | Common:1; Rare:114; Clinvar (benign):3 | ||||
| chr1:234373645-234373768 | Rare:49; Clinvar (benign):3 | ||||
| chr1:234607933-234608356 | Common:3; Rare:141 | ||||
| chr1:234608466-234608681 | Common:2; Rare:110; Clinvar (benign):2 | ||||
| chr1:235128801-235129060 | Common:1; Rare:101 | ||||
| chr1:235328142-235328617 | Common:4; Rare:147 | ||||
| chr1:235866847-235867150 | Common:3; Rare:89 | ||||
| chr1:236064995-236065348 | Common:2; Rare:130; Clinvar (pathogenic):1 | ||||
| chr1:236281871-236282249 | Common:7; Rare:113 | ||||
| chr1:236523867-236524041 | Common:2; Rare:44 | ||||
| chr1:236541379-236541702 | Common:13; Rare:77 | ||||
| chr1:236604462-236604657 | Common:4; Rare:58 | ||||
| chr1:239386472-239386676 | Rare:29 | ||||
| chr1:239719102-239719132 | Rare:1 |