| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:22625320-22625447 | Common:1; Rare:31 | ||||
| chr12:23949659-23949876 | Common:4; Rare:35 | ||||
| chr12:24903300-24903317 | Rare:1 | ||||
| chr12:24903515-24903583 | Rare:12 | ||||
| chr12:24948414-24948583 | Rare:35 | ||||
| chr12:24948610-24948793 | Common:3; Rare:21 | ||||
| chr12:24948838-24949296 | Common:5; Rare:111 | ||||
| chr12:25195053-25195438 | Common:2; Rare:120 | ||||
| chr12:25250430-25250555 | Rare:37 | ||||
| chr12:25250801-25251081 | Rare:93; Clinvar:5; Clinvar (benign):4 | ||||
| chr12:25958412-25958695 | Common:1; Rare:105 | ||||
| chr12:25958742-25958859 | Common:3; Rare:40 | ||||
| chr12:25958872-25958914 | Rare:14 | ||||
| chr12:25959096-25959159 | Rare:27 | ||||
| chr12:25959345-25959382 | Common:1; Rare:12 |