| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10812278-10812700 | Common:3; Rare:120 | ||||
| chr3:12618408-12619151 | Common:3; Rare:281; Clinvar:13; Clinvar (benign):15 | ||||
| chr3:12964600-12965140 | Common:3; Rare:189 | ||||
| chr3:12994089-12994406 | Common:2; Rare:71 | ||||
| chr3:13281510-13281930 | Common:2; Rare:156 | ||||
| chr3:13451777-13451995 | Common:2; Rare:104 | ||||
| chr3:16252220-16252490 | Common:4; Rare:84 | ||||
| chr3:20320450-20320984 | Common:5; Rare:139 | ||||
| chr3:24522338-24522586 | Common:2; Rare:63 | ||||
| chr3:27360360-27361000 | Rare:180 | ||||
| chr3:27452220-27452460 | Common:1; Rare:51 | ||||
| chr3:30349440-30349840 | Common:4; Rare:132 | ||||
| chr3:30607927-30608607 | Common:7; Rare:177 | ||||
| chr3:30622920-30623501 | Common:2; Rare:157; Clinvar:8; Clinvar (benign):11 | ||||
| chr3:31288664-31288961 | Common:7; Rare:110 |