| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169584328-169584415 | Rare:44 | ||||
| chr2:169584744-169584809 | Rare:15 | ||||
| chr2:169798795-169798965 | Rare:43 | ||||
| chr2:171433955-171434215 | Common:2; Rare:71 | ||||
| chr2:171522324-171522525 | Common:2; Rare:44 | ||||
| chr2:171687965-171688033 | Common:1; Rare:13 | ||||
| chr2:171894217-171894338 | Rare:57; Clinvar:1 | ||||
| chr2:171999837-171999964 | Common:1; Rare:55 | ||||
| chr2:174248468-174248758 | Common:1; Rare:90 | ||||
| chr2:174395617-174395812 | Common:2; Rare:62 | ||||
| chr2:175181654-175181762 | Common:3; Rare:48 | ||||
| chr2:177212441-177212821 | Common:4; Rare:152 | ||||
| chr2:177263410-177263703 | Common:1; Rare:68 | ||||
| chr2:177264597-177264826 | Common:2; Rare:72 | ||||
| chr2:177392659-177392858 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2 |