Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:190880605-190880900 | Common:4; Rare:99 | ||||
chr2:191014087-191014353 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191245207-191245487 | Common:2; Rare:92 | ||||
chr2:191677830-191678201 | Common:4; Rare:105 | ||||
chr2:191846915-191847299 | Rare:84 | ||||
chr2:192194900-192195033 | Rare:26 | ||||
chr2:197434970-197435186 | Rare:73 | ||||
chr2:197453355-197453571 | Rare:82 | ||||
chr2:197499794-197500453 | Common:1; Rare:252; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197515835-197516107 | Common:2; Rare:98 | ||||
chr2:197804918-197805264 | Common:4; Rare:74 | ||||
chr2:199851141-199851213 | Rare:30 | ||||
chr2:200509907-200510140 | Common:1; Rare:84 | ||||
chr2:200609105-200609367 | Rare:65 | ||||
chr2:200811407-200811596 | Common:1; Rare:64 |