| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:25195104-25195299 | Common:2; Rare:58 | ||||
| chr12:26937936-26938174 | Common:8; Rare:67 | ||||
| chr12:26938285-26938527 | Common:3; Rare:90 | ||||
| chr12:27523990-27524287 | Rare:69 | ||||
| chr12:27710565-27710875 | Common:5; Rare:103 | ||||
| chr12:28190378-28190493 | Common:1; Rare:35 | ||||
| chr12:30754744-30755064 | Common:1; Rare:127 | ||||
| chr12:31729015-31729267 | Rare:74 | ||||
| chr12:31959262-31959482 | Common:2; Rare:70 | ||||
| chr12:32679107-32679358 | Common:1; Rare:103; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755248-32755371 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:32755477-32755540 | Rare:22; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:32896738-32896979 | Common:2; Rare:79; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:38905566-38905789 | Common:5; Rare:59 | ||||
| chr12:42238176-42238471 | Common:1; Rare:98 |