| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174409913-174410160 | Common:6; Rare:47 | ||||
| chr2:174410305-174410372 | Common:3; Rare:17 | ||||
| chr2:174486977-174487409 | Common:2; Rare:108 | ||||
| chr2:175005135-175005294 | Rare:52; Clinvar:2 | ||||
| chr2:175167671-175167712 | Rare:17 | ||||
| chr2:175167876-175167915 | Rare:6 | ||||
| chr2:175168104-175168553 | Common:2; Rare:116 | ||||
| chr2:175181403-175181833 | Common:7; Rare:140 | ||||
| chr2:176002225-176002445 | Common:4; Rare:88 | ||||
| chr2:176002806-176002961 | Common:1; Rare:24 | ||||
| chr2:176269274-176269536 | Common:1; Rare:98 | ||||
| chr2:177212416-177212817 | Common:4; Rare:162 | ||||
| chr2:177263447-177263736 | Common:2; Rare:67 | ||||
| chr2:177264630-177264863 | Common:2; Rare:76 | ||||
| chr2:177392651-177392823 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 |