| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12725262-12725404 | Common:1; Rare:42 | ||||
| chr12:12927532-12927778 | Common:5; Rare:77 | ||||
| chr12:15163028-15163789 | Common:6; Rare:127 | ||||
| chr12:15220559-15220728 | Rare:21 | ||||
| chr12:15688501-15688540 | Rare:6 | ||||
| chr12:16349142-16349449 | Common:2; Rare:55 | ||||
| chr12:21852290-21852412 | Common:2; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:25958209-25958246 | Rare:11 | ||||
| chr12:26126117-26126160 | Rare:18 | ||||
| chr12:26957522-26957712 | Rare:51 | ||||
| chr12:30795648-30795738 | Common:1; Rare:22 | ||||
| chr12:31749209-31749397 | Common:1; Rare:30 | ||||
| chr12:46383139-46383463 | Common:1; Rare:126 | ||||
| chr12:46383895-46384081 | Common:1; Rare:55 | ||||
| chr12:47080799-47080913 | Common:1; Rare:37 |