| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113135685-113135997 | Common:1; Rare:46 | ||||
| chr12:113165645-113165952 | Rare:112 | ||||
| chr12:113185384-113185777 | Common:10; Rare:153 | ||||
| chr12:113221071-113221319 | Common:1; Rare:77 | ||||
| chr12:114684146-114684463 | Common:1; Rare:83 | ||||
| chr12:117361147-117361228 | Rare:23 | ||||
| chr12:118016489-118016780 | Common:3; Rare:57 | ||||
| chr12:118061044-118061223 | Common:1; Rare:52 | ||||
| chr12:118135938-118136219 | Common:2; Rare:91 | ||||
| chr12:118372854-118373165 | Common:2; Rare:81 | ||||
| chr12:118376339-118376712 | Common:1; Rare:108 | ||||
| chr12:118376722-118376773 | Rare:14 | ||||
| chr12:119178615-119178944 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:119179334-119179558 | Rare:79; Clinvar:7; Clinvar (benign):3 | ||||
| chr12:119668105-119668163 | Common:1; Rare:9 |