| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207625216-207625379 | Common:1; Rare:50 | ||||
| chr2:208255013-208255234 | Common:2; Rare:57 | ||||
| chr2:208266064-208266302 | Common:8; Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209424164-209424404 | Common:1; Rare:51 | ||||
| chr2:210477573-210477690 | Rare:39 | ||||
| chr2:213148723-213148818 | Rare:19 | ||||
| chr2:213152260-213152322 | Rare:15 | ||||
| chr2:213284187-213284521 | Rare:112 | ||||
| chr2:214809583-214809991 | Common:5; Rare:147; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:215138169-215138391 | Rare:43; Clinvar:1 | ||||
| chr2:215138394-215138753 | Common:2; Rare:70 | ||||
| chr2:215311853-215312160 | Common:8; Rare:120 | ||||
| chr2:216081745-216081906 | Common:1; Rare:53 | ||||
| chr2:216498740-216498904 | Common:6; Rare:72 | ||||
| chr2:216694459-216694506 | Rare:7 |