| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134253289-134253608 | Common:2; Rare:117; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:134276195-134276318 | Common:2; Rare:18 | ||||
| chr11:134331662-134332077 | Common:10; Rare:98 | ||||
| chr12:389023-389364 | Common:5; Rare:164 | ||||
| chr12:389453-389693 | Common:5; Rare:104 | ||||
| chr12:401400-401685 | Common:2; Rare:80 | ||||
| chr12:949510-949994 | Common:8; Rare:132 | ||||
| chr12:991050-991266 | Common:2; Rare:83 | ||||
| chr12:1690838-1691172 | Common:3; Rare:122 | ||||
| chr12:1800775-1800862 | Common:1; Rare:21 | ||||
| chr12:2004400-2004723 | Common:2; Rare:108 | ||||
| chr12:2796909-2797240 | Rare:76 | ||||
| chr12:2812410-2812752 | Common:1; Rare:91 | ||||
| chr12:2812884-2813057 | Rare:48 | ||||
| chr12:2877022-2877262 | Rare:71 |