| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:153163277-153163593 | Rare:78 | ||||
| chr3:157089159-157089247 | Rare:34 | ||||
| chr3:157174861-157175223 | Common:3; Rare:157 | ||||
| chr3:169765038-169765222 | Rare:77; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:179452304-179452459 | Rare:23 | ||||
| chr3:181174747-181175116 | Common:1; Rare:57 | ||||
| chr3:181699141-181699462 | Rare:45 | ||||
| chr3:181699469-181699793 | Common:1; Rare:56 | ||||
| chr3:181713116-181713231 | Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183447389-183447814 | Common:4; Rare:100 | ||||
| chr3:192514743-192514969 | Rare:51 | ||||
| chr3:192515315-192515379 | Common:1; Rare:12 | ||||
| chr3:194583872-194584021 | Common:10; Rare:55 | ||||
| chr3:195657926-195658126 | Common:11; Rare:36 | ||||
| chr3:195990216-195990427 | Rare:25 |