| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171522262-171522538 | Common:3; Rare:66 | ||||
| chr2:171687655-171687932 | Rare:80 | ||||
| chr2:171687989-171688026 | Rare:6 | ||||
| chr2:171894217-171894342 | Rare:57; Clinvar:1 | ||||
| chr2:171999831-171999975 | Common:1; Rare:60 | ||||
| chr2:172427363-172427702 | Common:9; Rare:99; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:173354557-173354947 | Common:1; Rare:121 | ||||
| chr2:173964006-173964320 | Rare:124 | ||||
| chr2:173965215-173965515 | Common:1; Rare:104 | ||||
| chr2:174248454-174248744 | Common:1; Rare:87 | ||||
| chr2:174395594-174395876 | Common:2; Rare:91 | ||||
| chr2:174486958-174487355 | Common:2; Rare:92 | ||||
| chr2:175005172-175005331 | Rare:56; Clinvar:2 | ||||
| chr2:175168104-175168580 | Common:2; Rare:128 | ||||
| chr2:175181629-175181755 | Common:4; Rare:59 |