| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:175181654-175181764 | Common:3; Rare:48 | ||||
| chr2:176002254-176002394 | Common:1; Rare:53 | ||||
| chr2:177212445-177212809 | Common:4; Rare:146 | ||||
| chr2:177213142-177213272 | Rare:57 | ||||
| chr2:177264646-177264714 | Common:1; Rare:28 | ||||
| chr2:177392657-177392823 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:178450696-178450874 | Common:1; Rare:61 | ||||
| chr2:178451098-178451379 | Common:5; Rare:82; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:178478527-178478719 | Common:1; Rare:63 | ||||
| chr2:180007080-180007376 | Common:1; Rare:71 | ||||
| chr2:183078680-183078792 | Rare:20 | ||||
| chr2:183124120-183124460 | Common:5; Rare:94 | ||||
| chr2:186486130-186486364 | Common:3; Rare:82 | ||||
| chr2:188291642-188292093 | Common:5; Rare:126 | ||||
| chr2:188292692-188292944 | Common:1; Rare:59 |