| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128879293-128879714 | Common:31; Rare:1048; Clinvar:14; Clinvar (benign):20; Clinvar (pathogenic):2 | ||||
| chr3:128991672-128992142 | Common:9; Rare:219 | ||||
| chr3:128993968-128994368 | Common:3; Rare:157 | ||||
| chr3:129001060-129001420 | Common:3; Rare:89 | ||||
| chr3:129121552-129122450 | Common:5; Rare:219 | ||||
| chr3:129160855-129161568 | Common:61; Rare:993 | ||||
| chr3:129161560-129161980 | Common:4; Rare:145 | ||||
| chr3:129183669-129184222 | Common:16; Rare:911 | ||||
| chr3:129249102-129249729 | Common:19; Rare:526 | ||||
| chr3:129278598-129279045 | Common:23; Rare:460 | ||||
| chr3:129279050-129279380 | Common:2; Rare:70 | ||||
| chr3:129315800-129317010 | Common:33; Rare:981 | ||||
| chr3:129428459-129428882 | Common:11; Rare:363 | ||||
| chr3:129439341-129440487 | Common:15; Rare:1449; Clinvar:15; Clinvar (benign):7 | ||||
| chr3:129440500-129440670 | Rare:71 |