| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:11746475-11746648 | Common:1; Rare:54; Clinvar:2 | ||||
| chr2:12716620-12717005 | Common:3; Rare:119 | ||||
| chr2:15561298-15561443 | Rare:55 | ||||
| chr2:15940351-15940563 | Rare:52 | ||||
| chr2:16665798-16665989 | Common:4; Rare:39 | ||||
| chr2:17540424-17540798 | Common:2; Rare:82 | ||||
| chr2:17753731-17754177 | Common:4; Rare:142; Clinvar (benign):1 | ||||
| chr2:19901652-19901746 | Common:1; Rare:47 | ||||
| chr2:19901949-19902037 | Common:1; Rare:27 | ||||
| chr2:19990018-19990223 | Rare:61 | ||||
| chr2:20051485-20051874 | Common:1; Rare:111 | ||||
| chr2:20350324-20350434 | Common:1; Rare:40 | ||||
| chr2:20651053-20651312 | Common:1; Rare:79 | ||||
| chr2:20823055-20823186 | Common:1; Rare:48 | ||||
| chr2:23927073-23927295 | Common:3; Rare:80 |