| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169147281-169147525 | Common:2; Rare:55 | ||||
| chr3:169772714-169772797 | Common:1; Rare:21 | ||||
| chr3:169773331-169773425 | Rare:30 | ||||
| chr3:169966706-169966836 | Rare:54 | ||||
| chr3:170222339-170222531 | Common:1; Rare:68 | ||||
| chr3:170418649-170418940 | Common:2; Rare:64 | ||||
| chr3:170870163-170870312 | Rare:76 | ||||
| chr3:172039494-172039656 | Common:1; Rare:52 | ||||
| chr3:172711003-172711396 | Common:1; Rare:111 | ||||
| chr3:179347640-179347792 | Common:1; Rare:41 | ||||
| chr3:179562669-179563009 | Rare:110 | ||||
| chr3:179604605-179604873 | Common:2; Rare:106 | ||||
| chr3:180989618-180989829 | Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:184017910-184018103 | Common:1; Rare:59 | ||||
| chr3:184135093-184135418 | Common:2; Rare:91; Clinvar:5 |