| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126355534-126355785 | Common:1; Rare:69 | ||||
| chr11:128693954-128694141 | Rare:30 | ||||
| chr11:130069279-130069521 | Common:3; Rare:49 | ||||
| chr11:130448426-130448647 | Rare:52 | ||||
| chr11:134253278-134253586 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr12:389300-389375 | Rare:28 | ||||
| chr12:991101-991229 | Common:1; Rare:50 | ||||
| chr12:2812533-2812702 | Common:1; Rare:40 | ||||
| chr12:2877003-2877262 | Rare:77 | ||||
| chr12:4648988-4649132 | Common:1; Rare:41 | ||||
| chr12:6451735-6452141 | Common:4; Rare:71 | ||||
| chr12:6493239-6493386 | Common:5; Rare:41 | ||||
| chr12:6534385-6534572 | Common:5; Rare:81 | ||||
| chr12:6723855-6724178 | Common:1; Rare:68 | ||||
| chr12:6873274-6873495 | Common:2; Rare:62 |