| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:25195084-25195286 | Common:2; Rare:64 | ||||
| chr12:26937961-26938708 | Common:12; Rare:249 | ||||
| chr12:27022413-27022569 | Common:2; Rare:41 | ||||
| chr12:27244029-27244319 | Common:2; Rare:93 | ||||
| chr12:27710733-27710886 | Common:2; Rare:67 | ||||
| chr12:29149144-29149358 | Rare:61 | ||||
| chr12:31729019-31729292 | Common:1; Rare:82 | ||||
| chr12:31959242-31959477 | Common:2; Rare:75 | ||||
| chr12:32485760-32486083 | Rare:55 | ||||
| chr12:38905437-38905719 | Common:4; Rare:77 | ||||
| chr12:40224888-40225095 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:42326071-42326225 | Common:1; Rare:47 | ||||
| chr12:43758753-43759007 | Common:2; Rare:72; Clinvar:2 | ||||
| chr12:45215982-45216120 | Common:1; Rare:48 | ||||
| chr12:45990510-45990926 | Common:2; Rare:134 |