| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171999831-171999996 | Common:1; Rare:68 | ||||
| chr2:173965350-173965513 | Common:1; Rare:68 | ||||
| chr2:174248456-174248751 | Common:1; Rare:91 | ||||
| chr2:174395619-174395800 | Common:2; Rare:59 | ||||
| chr2:175168306-175168570 | Common:1; Rare:66 | ||||
| chr2:175181659-175181846 | Common:3; Rare:62 | ||||
| chr2:176002229-176002340 | Common:2; Rare:51 | ||||
| chr2:176116603-176116810 | Common:2; Rare:48 | ||||
| chr2:176188500-176188678 | Common:1; Rare:70 | ||||
| chr2:176188911-176189106 | Common:2; Rare:67 | ||||
| chr2:176269196-176269505 | Common:2; Rare:99 | ||||
| chr2:177212383-177212821 | Common:5; Rare:177 | ||||
| chr2:177263432-177263703 | Common:1; Rare:65 | ||||
| chr2:177264612-177264863 | Common:2; Rare:79 | ||||
| chr2:177392634-177393005 | Common:3; Rare:126; Clinvar:6; Clinvar (benign):4 |