| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219176780-219177220 | Common:29; Rare:509 | ||||
| chr2:219177635-219178390 | Common:52; Rare:697 | ||||
| chr2:219178540-219178850 | Common:1; Rare:253 | ||||
| chr2:219206550-219206972 | Rare:718 | ||||
| chr2:219206918-219207346 | Common:14; Rare:394 | ||||
| chr2:219217771-219218171 | Common:4; Rare:141; Clinvar:2 | ||||
| chr2:219218880-219219330 | Common:6; Rare:318 | ||||
| chr2:219229160-219229470 | Common:2; Rare:163 | ||||
| chr2:219229490-219230070 | Common:17; Rare:844 | ||||
| chr2:219230210-219230610 | Rare:158 | ||||
| chr2:219231978-219232378 | Common:4; Rare:191 | ||||
| chr2:219245220-219245611 | Common:7; Rare:314 | ||||
| chr2:219252818-219253571 | Common:10; Rare:361 | ||||
| chr2:219253800-219254200 | Common:7; Rare:284 | ||||
| chr2:219277631-219278031 | Common:3; Rare:141 |