| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216694438-216694858 | Rare:102 | ||||
| chr2:216695005-216695074 | Rare:15 | ||||
| chr2:216695099-216695557 | Common:2; Rare:77 | ||||
| chr2:217434146-217434357 | Rare:45 | ||||
| chr2:217858556-217858690 | Rare:14 | ||||
| chr2:217901881-217902156 | Common:3; Rare:47 | ||||
| chr2:217978770-217978935 | Common:1; Rare:47 | ||||
| chr2:218002857-218003115 | Common:2; Rare:66 | ||||
| chr2:218217058-218217246 | Common:1; Rare:67 | ||||
| chr2:218270057-218270591 | Common:5; Rare:169; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218279036-218279355 | Common:2; Rare:92 | ||||
| chr2:218281994-218282334 | Common:5; Rare:97; Clinvar (benign):1 | ||||
| chr2:218286739-218286898 | Common:1; Rare:28 | ||||
| chr2:218287231-218287376 | Rare:26 | ||||
| chr2:218322953-218323361 | Common:7; Rare:137 |