| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:24902260-24902587 | Common:4; Rare:57 | ||||
| chr12:25195132-25195308 | Common:2; Rare:51 | ||||
| chr12:26938267-26938534 | Common:3; Rare:101 | ||||
| chr12:27523989-27524249 | Rare:62 | ||||
| chr12:27710738-27710853 | Common:1; Rare:45 | ||||
| chr12:28190378-28190488 | Common:1; Rare:31 | ||||
| chr12:29149071-29149347 | Rare:80 | ||||
| chr12:29381119-29381293 | Common:2; Rare:65 | ||||
| chr12:30695860-30695985 | Common:1; Rare:31 | ||||
| chr12:30754753-30755031 | Common:1; Rare:107 | ||||
| chr12:31073738-31073896 | Common:7; Rare:60 | ||||
| chr12:31728995-31729267 | Rare:81 | ||||
| chr12:31959282-31959482 | Common:2; Rare:62 | ||||
| chr12:32106565-32106908 | Common:5; Rare:95 | ||||
| chr12:32679107-32679359 | Common:1; Rare:104; Clinvar:1; Clinvar (benign):4 |