| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:182793360-182793604 | Common:3; Rare:64 | ||||
| chr3:183099406-183099742 | Common:2; Rare:111; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183635497-183635753 | Common:4; Rare:70 | ||||
| chr3:183697680-183697917 | Common:2; Rare:105 | ||||
| chr3:184017868-184018125 | Common:1; Rare:82 | ||||
| chr3:184135221-184135392 | Common:2; Rare:52; Clinvar:5 | ||||
| chr3:184185914-184186233 | Common:4; Rare:123 | ||||
| chr3:184249507-184249691 | Rare:47 | ||||
| chr3:184298947-184299279 | Common:3; Rare:102 | ||||
| chr3:184362165-184362242 | Common:1; Rare:11 | ||||
| chr3:184711944-184712272 | Common:1; Rare:107 | ||||
| chr3:185282855-185283015 | Common:1; Rare:40 | ||||
| chr3:185498923-185499162 | Rare:87 | ||||
| chr3:185585967-185586358 | Common:1; Rare:90 | ||||
| chr3:185823253-185823314 | Rare:21 |