| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16512862-16512952 | Rare:21 | ||||
| chr3:16513416-16513973 | Common:4; Rare:164 | ||||
| chr3:16884866-16885260 | Common:7; Rare:100 | ||||
| chr3:17742500-17742952 | Common:4; Rare:158 | ||||
| chr3:18424230-18424472 | Common:5; Rare:52 | ||||
| chr3:18438729-18438820 | Rare:11 | ||||
| chr3:18444739-18444976 | Rare:49 | ||||
| chr3:18445548-18445821 | Common:3; Rare:57 | ||||
| chr3:19946954-19947450 | Common:7; Rare:185 | ||||
| chr3:20186147-20186548 | Common:6; Rare:123 | ||||
| chr3:23916866-23917208 | Rare:134 | ||||
| chr3:23917648-23918012 | Common:2; Rare:95; Clinvar (benign):1 | ||||
| chr3:24494722-24494903 | Rare:47 | ||||
| chr3:25428106-25428398 | Rare:66 | ||||
| chr3:25664308-25664629 | Common:1; Rare:92 |