| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:153162883-153162949 | Rare:15 | ||||
| chr3:153163436-153163477 | Rare:13 | ||||
| chr3:156816952-156817115 | Common:1; Rare:67 | ||||
| chr3:157088690-157088806 | Common:1; Rare:29 | ||||
| chr3:157174851-157175263 | Common:3; Rare:181 | ||||
| chr3:169764839-169765117 | Common:1; Rare:97; Clinvar:18; Clinvar (pathogenic):5 | ||||
| chr3:184317314-184317814 | Common:2; Rare:135 | ||||
| chr3:184322700-184322954 | Rare:64 | ||||
| chr3:184710913-184711093 | Common:1; Rare:66 | ||||
| chr3:185465675-185465827 | Common:2; Rare:43 | ||||
| chr3:187739866-187740001 | Common:1; Rare:24 | ||||
| chr3:187742609-187742731 | Common:1; Rare:18 | ||||
| chr3:187747119-187747320 | Rare:32 | ||||
| chr3:192408057-192408091 | Rare:7 | ||||
| chr3:192408113-192408321 | Rare:60 |