| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139354607-139354640 | Common:1; Rare:4 | ||||
| chr3:141660276-141660339 | Rare:18 | ||||
| chr3:150408869-150409008 | Rare:43 | ||||
| chr3:150409068-150409268 | Rare:38 | ||||
| chr3:152203763-152203936 | Common:2; Rare:27 | ||||
| chr3:155293670-155293755 | Common:2; Rare:13 | ||||
| chr3:157174870-157175223 | Common:3; Rare:154 | ||||
| chr3:159732283-159732396 | Common:1; Rare:19 | ||||
| chr3:167811060-167811208 | Rare:22 | ||||
| chr3:169765038-169765264 | Rare:85; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:183447441-183447674 | Common:2; Rare:57 | ||||
| chr3:185418803-185418947 | Rare:15 | ||||
| chr3:194583904-194584020 | Common:4; Rare:40 | ||||
| chr3:195657911-195658126 | Common:12; Rare:37 | ||||
| chr3:195990224-195990414 | Rare:23 |