Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:232420088-232420278 | Common:1; Rare:42 | ||||
chr2:232420916-232421059 | Common:1; Rare:38 | ||||
chr2:232421297-232421678 | Common:4; Rare:67 | ||||
chr2:232585761-232585774 | Rare:3 | ||||
chr2:232790761-232791093 | Rare:93; Clinvar:1 | ||||
chr2:233139540-233139784 | Rare:28 | ||||
chr2:234495968-234496092 | Rare:35 | ||||
chr2:234682991-234683025 | Rare:13 | ||||
chr2:237359245-237359419 | Rare:48; Clinvar:4; Clinvar (benign):2 | ||||
chr2:238081028-238081155 | Rare:26 | ||||
chr2:238231651-238231809 | Common:3; Rare:55 | ||||
chr2:238328693-238329041 | Common:2; Rare:109; Clinvar (pathogenic):2 | ||||
chr2:240778768-240778835 | Common:1; Rare:15 | ||||
chr2:241166986-241167071 | Rare:32 | ||||
chr2:241327103-241327409 | Common:1; Rare:67 |