| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:235367210-235367514 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:235367630-235367772 | Rare:48 | ||||
| chr1:235503851-235503999 | Common:5; Rare:43 | ||||
| chr1:235504357-235504861 | Common:14; Rare:383 | ||||
| chr1:235504923-235505260 | Common:1; Rare:72 | ||||
| chr1:235866820-235867201 | Common:6; Rare:199 | ||||
| chr1:235882760-235883120 | Common:2; Rare:78 | ||||
| chr1:236142162-236142592 | Common:18; Rare:224 | ||||
| chr1:236281835-236282303 | Common:13; Rare:214 | ||||
| chr1:236394773-236395496 | Rare:161 | ||||
| chr1:236395830-236396220 | Common:2; Rare:80 | ||||
| chr1:236516939-236517726 | Common:7; Rare:160 | ||||
| chr1:236523181-236523490 | Common:4; Rare:107 | ||||
| chr1:236523682-236524059 | Common:10; Rare:195 | ||||
| chr1:236524433-236524632 | Common:4; Rare:94 |