| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:22046189-22046389 | Rare:53 | ||||
| chr12:22334765-22336064 | Common:8; Rare:432 | ||||
| chr12:22436840-22437680 | Common:8; Rare:217 | ||||
| chr12:22544120-22544410 | Common:3; Rare:315 | ||||
| chr12:22544378-22544753 | Common:6; Rare:228 | ||||
| chr12:22624975-22625302 | Common:1; Rare:268 | ||||
| chr12:22625524-22625941 | Common:6; Rare:158 | ||||
| chr12:24948910-24949290 | Common:4; Rare:93 | ||||
| chr12:25195102-25195420 | Common:6; Rare:211 | ||||
| chr12:25250849-25251346 | Rare:288; Clinvar:10; Clinvar (benign):7 | ||||
| chr12:25958434-25959310 | Common:19; Rare:686 | ||||
| chr12:25959385-25959884 | Common:12; Rare:144 | ||||
| chr12:26124977-26125262 | Common:2; Rare:128 | ||||
| chr12:26195430-26195680 | Common:12; Rare:78 | ||||
| chr12:26195918-26196097 | Common:1; Rare:41 |