| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129316245-129316485 | Common:1; Rare:76 | ||||
| chr3:129316510-129316830 | Common:3; Rare:56 | ||||
| chr3:129428601-129428839 | Common:2; Rare:68 | ||||
| chr3:129439916-129440455 | Common:5; Rare:170; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129572846-129573246 | Common:4; Rare:132 | ||||
| chr3:129606725-129607125 | Common:4; Rare:152 | ||||
| chr3:129688080-129688535 | Common:1; Rare:112 | ||||
| chr3:129688490-129688916 | Common:7; Rare:246 | ||||
| chr3:129893142-129893312 | Common:1; Rare:55 | ||||
| chr3:129893544-129893906 | Rare:140 | ||||
| chr3:130746750-130747004 | Common:3; Rare:69 | ||||
| chr3:130893876-130894103 | Common:2; Rare:70 | ||||
| chr3:131381477-131381866 | Common:3; Rare:113 | ||||
| chr3:131502798-131503111 | Common:1; Rare:114 | ||||
| chr3:132417149-132417315 | Common:3; Rare:71 |