| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38138750-38139540 | Rare:248; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:38164354-38165301 | Common:11; Rare:799 | ||||
| chr3:38165240-38166233 | Common:11; Rare:1015 | ||||
| chr3:38346639-38347067 | Common:1; Rare:324 | ||||
| chr3:38347162-38347562 | Common:4; Rare:85 | ||||
| chr3:38453500-38454040 | Common:3; Rare:424 | ||||
| chr3:38454164-38454873 | Common:7; Rare:561 | ||||
| chr3:38496070-38496500 | Common:2; Rare:163 | ||||
| chr3:38496402-38497044 | Common:5; Rare:443 | ||||
| chr3:38649476-38649954 | Common:25; Rare:519; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:39051720-39052120 | Common:8; Rare:409 | ||||
| chr3:39052261-39052661 | Common:5; Rare:265 | ||||
| chr3:39106872-39107272 | Common:12; Rare:234 | ||||
| chr3:39107370-39108095 | Common:26; Rare:454 | ||||
| chr3:39153467-39153881 | Common:35; Rare:749 |