| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68734752-68734801 | Common:1; Rare:8 | ||||
| chr2:68735002-68735116 | Common:1; Rare:20 | ||||
| chr2:68774757-68774947 | Rare:33 | ||||
| chr2:69387207-69387412 | Rare:62; Clinvar:2 | ||||
| chr2:69437428-69437479 | Rare:17; Clinvar (benign):1 | ||||
| chr2:69829501-69829741 | Common:1; Rare:98 | ||||
| chr2:69893887-69894013 | Rare:34 | ||||
| chr2:70086909-70087116 | Common:1; Rare:106 | ||||
| chr2:70087412-70087746 | Rare:132 | ||||
| chr2:70190971-70191124 | Rare:35 | ||||
| chr2:70248543-70248762 | Common:4; Rare:91 | ||||
| chr2:70257978-70258158 | Common:1; Rare:60 | ||||
| chr2:70293661-70293902 | Common:3; Rare:76 | ||||
| chr2:71068526-71068654 | Rare:64 | ||||
| chr2:71130224-71130662 | Common:6; Rare:122; Clinvar:1; Clinvar (benign):2 |