| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157174840-157175263 | Common:3; Rare:184 | ||||
| chr3:158670963-158671069 | Common:3; Rare:23 | ||||
| chr3:169765029-169765274 | Rare:92; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr3:170699516-170699713 | Common:2; Rare:42 | ||||
| chr3:185418805-185419109 | Common:1; Rare:44 | ||||
| chr3:185656427-185656712 | Rare:58 | ||||
| chr3:187738847-187739099 | Common:2; Rare:51 | ||||
| chr3:187742398-187742416 | Rare:1 | ||||
| chr3:187743278-187743573 | Common:3; Rare:78 | ||||
| chr3:187744044-187744282 | Rare:78 | ||||
| chr3:188951066-188951174 | Rare:19 | ||||
| chr3:189099081-189099465 | Rare:91 | ||||
| chr3:194583866-194584027 | Common:11; Rare:56 | ||||
| chr3:195657920-195658137 | Common:12; Rare:37 | ||||
| chr3:195688217-195688553 | Common:2; Rare:29 |