| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152320177-152320479 | Rare:56 | ||||
| chr3:157174851-157175253 | Common:3; Rare:174 | ||||
| chr3:169764853-169765036 | Common:1; Rare:58; Clinvar:15; Clinvar (pathogenic):4 | ||||
| chr3:169765044-169765252 | Rare:82; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:172247709-172247822 | Rare:39 | ||||
| chr3:179225892-179226005 | Rare:22; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:187742553-187742777 | Common:1; Rare:37 | ||||
| chr3:188198918-188199156 | Common:1; Rare:32 | ||||
| chr3:188266133-188266369 | Rare:48 | ||||
| chr3:188299410-188299577 | Common:3; Rare:32 | ||||
| chr3:188791959-188792170 | Rare:46 | ||||
| chr3:194583866-194584026 | Common:11; Rare:56 | ||||
| chr3:195571294-195571621 | Common:3; Rare:80 | ||||
| chr3:195657926-195658131 | Common:11; Rare:37 | ||||
| chr3:195990233-195990427 | Rare:24 |