| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200889030-200889445 | Common:3; Rare:133 | ||||
| chr2:200963594-200963871 | Common:1; Rare:73 | ||||
| chr2:201071598-201072039 | Rare:98 | ||||
| chr2:201115740-201116029 | Rare:64 | ||||
| chr2:201118604-201118831 | Rare:34 | ||||
| chr2:201451379-201451816 | Common:2; Rare:115 | ||||
| chr2:201642653-201642736 | Rare:44 | ||||
| chr2:201780890-201781227 | Common:2; Rare:105; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238443-202238615 | Rare:60; Clinvar:1 | ||||
| chr2:202265620-202265824 | Rare:77 | ||||
| chr2:202912147-202912298 | Common:1; Rare:53 | ||||
| chr2:202912474-202912560 | Common:2; Rare:29 | ||||
| chr2:203014643-203014931 | Common:1; Rare:92 | ||||
| chr2:203238719-203239080 | Common:3; Rare:124 | ||||
| chr2:203239222-203239320 | Rare:32 |