| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:28190884-28190952 | Common:1; Rare:18 | ||||
| chr12:30695661-30695738 | Rare:27 | ||||
| chr12:30695794-30696002 | Common:2; Rare:56 | ||||
| chr12:31073780-31073874 | Rare:36 | ||||
| chr12:31074085-31074285 | Common:1; Rare:39 | ||||
| chr12:31325894-31326245 | Common:4; Rare:88 | ||||
| chr12:31729019-31729267 | Rare:72 | ||||
| chr12:31959302-31959461 | Common:2; Rare:52 | ||||
| chr12:32107078-32107190 | Rare:25 | ||||
| chr12:32107218-32107340 | Common:2; Rare:32 | ||||
| chr12:32739923-32740132 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:32755221-32755315 | Common:1; Rare:25; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:32755414-32755618 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:32755827-32755969 | Rare:60 | ||||
| chr12:42144428-42144693 | Common:8; Rare:109 |