| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:128693948-128694169 | Rare:38 | ||||
| chr11:129279511-129279738 | Common:3; Rare:97 | ||||
| chr11:129895510-129895688 | Common:2; Rare:74 | ||||
| chr11:130314407-130314454 | Rare:20 | ||||
| chr11:134224533-134224723 | Rare:76 | ||||
| chr11:134253266-134253584 | Common:2; Rare:105; Clinvar (benign):1 | ||||
| chr12:389230-389364 | Rare:49 | ||||
| chr12:389529-389640 | Common:5; Rare:52 | ||||
| chr12:401443-401655 | Rare:57 | ||||
| chr12:752333-752605 | Common:1; Rare:79 | ||||
| chr12:991154-991281 | Rare:53 | ||||
| chr12:1592524-1592634 | Rare:29 | ||||
| chr12:2004389-2004670 | Common:2; Rare:100 | ||||
| chr12:2794855-2795157 | Common:1; Rare:101 | ||||
| chr12:2812577-2812740 | Common:1; Rare:56 |