| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191245231-191245555 | Common:3; Rare:104 | ||||
| chr2:191677843-191678173 | Common:4; Rare:95 | ||||
| chr2:197434996-197435180 | Rare:61 | ||||
| chr2:197453244-197453561 | Rare:109 | ||||
| chr2:197499791-197500167 | Common:1; Rare:130; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197500243-197500430 | Common:1; Rare:75 | ||||
| chr2:199911104-199911349 | Rare:69 | ||||
| chr2:200510033-200510263 | Common:1; Rare:70 | ||||
| chr2:200609105-200609359 | Rare:63 | ||||
| chr2:200811408-200811596 | Common:1; Rare:63 | ||||
| chr2:200888994-200889424 | Common:2; Rare:138 | ||||
| chr2:201071615-201072039 | Rare:91 | ||||
| chr2:201451444-201451856 | Common:2; Rare:104 | ||||
| chr2:201642637-201642743 | Rare:53 | ||||
| chr2:201643435-201643553 | Rare:36; Clinvar:3; Clinvar (benign):1 |