| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:180989606-180989794 | Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:182793360-182793638 | Common:3; Rare:69 | ||||
| chr3:183099436-183099742 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183635488-183635745 | Common:4; Rare:72 | ||||
| chr3:184017876-184018053 | Rare:50 | ||||
| chr3:184135221-184135388 | Common:2; Rare:50; Clinvar:5 | ||||
| chr3:184185910-184186210 | Common:4; Rare:112 | ||||
| chr3:184249495-184249706 | Rare:58 | ||||
| chr3:184315011-184315319 | Common:1; Rare:89 | ||||
| chr3:184325330-184325613 | Common:1; Rare:79 | ||||
| chr3:184337376-184337606 | Rare:34 | ||||
| chr3:184711926-184712243 | Common:2; Rare:107 | ||||
| chr3:185282855-185283003 | Common:1; Rare:38 | ||||
| chr3:186567281-186567431 | Common:3; Rare:43 | ||||
| chr3:186783261-186783639 | Common:1; Rare:166 |