| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208266032-208266306 | Common:9; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002395-210002669 | Common:6; Rare:93 | ||||
| chr2:210476686-210476889 | Common:1; Rare:54 | ||||
| chr2:210477568-210477690 | Rare:39 | ||||
| chr2:213148750-213148813 | Rare:13 | ||||
| chr2:213150387-213150735 | Common:5; Rare:70 | ||||
| chr2:213151612-213151998 | Common:1; Rare:159 | ||||
| chr2:213152253-213152359 | Common:1; Rare:20 | ||||
| chr2:215311900-215312145 | Common:8; Rare:100 | ||||
| chr2:216081761-216081882 | Rare:35 | ||||
| chr2:216412675-216412788 | Rare:14 | ||||
| chr2:216498740-216498904 | Common:6; Rare:72 | ||||
| chr2:216694438-216694475 | Rare:6 | ||||
| chr2:216694504-216694858 | Rare:90 | ||||
| chr2:216695099-216695338 | Common:2; Rare:36 |