Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:33134417-33134665 | Common:2; Rare:50 | ||||
chr2:36356029-36356421 | Common:4; Rare:127 | ||||
chr2:37084269-37084568 | Common:4; Rare:113 | ||||
chr2:37231532-37231726 | Common:4; Rare:112; Clinvar (benign):4 | ||||
chr2:37671447-37671764 | Common:1; Rare:113 | ||||
chr2:37672881-37672940 | Rare:11 | ||||
chr2:38076131-38076282 | Rare:37 | ||||
chr2:38875897-38876041 | Common:1; Rare:48 | ||||
chr2:39120981-39121112 | Common:1; Rare:46 | ||||
chr2:39437039-39437456 | Common:4; Rare:146 | ||||
chr2:40452057-40452249 | Common:4; Rare:73 | ||||
chr2:42792727-42792978 | Common:1; Rare:65 | ||||
chr2:43595967-43596205 | Common:1; Rare:85 | ||||
chr2:44361483-44362005 | Common:3; Rare:165 | ||||
chr2:46356557-46356785 | Rare:42 |