| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9843957-9844080 | Common:2; Rare:58 | ||||
| chr3:9917017-9917169 | Common:1; Rare:29 | ||||
| chr3:9933503-9933863 | Common:2; Rare:145; Clinvar:3 | ||||
| chr3:9986778-9987163 | Common:3; Rare:108 | ||||
| chr3:10026304-10026473 | Rare:54 | ||||
| chr3:10321041-10321266 | Common:2; Rare:92 | ||||
| chr3:11154347-11154542 | Common:3; Rare:51 | ||||
| chr3:11719419-11719595 | Rare:57 | ||||
| chr3:12664058-12664300 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:13420222-13420445 | Common:1; Rare:63 | ||||
| chr3:13480029-13480339 | Common:2; Rare:75 | ||||
| chr3:14124713-14125179 | Common:4; Rare:137; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178876 | Common:2; Rare:158; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14402485-14402722 | Rare:55 | ||||
| chr3:14651409-14651681 | Common:1; Rare:75 |