| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113422310-113422446 | Common:4; Rare:57 | ||||
| chr12:113966273-113966532 | Common:12; Rare:140 | ||||
| chr12:114682706-114683300 | Common:2; Rare:188; Clinvar:7; Clinvar (benign):3 | ||||
| chr12:114683339-114683668 | Common:4; Rare:102; Clinvar:11; Clinvar (benign):7 | ||||
| chr12:114683865-114684447 | Common:9; Rare:268; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:114684401-114684681 | Common:3; Rare:145 | ||||
| chr12:116277539-116277714 | Rare:56 | ||||
| chr12:116737983-116738362 | Common:10; Rare:248 | ||||
| chr12:116878582-116878727 | Common:2; Rare:33 | ||||
| chr12:116878780-116879071 | Common:1; Rare:55 | ||||
| chr12:116880980-116881660 | Common:5; Rare:203 | ||||
| chr12:116910874-116911041 | Rare:109 | ||||
| chr12:117099375-117099532 | Common:2; Rare:80 | ||||
| chr12:118016541-118016820 | Common:4; Rare:102 | ||||
| chr12:118060774-118061030 | Common:2; Rare:112 |