Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:36513426-36513675 | Common:1; Rare:72 | ||||
chr2:36558446-36558697 | Common:2; Rare:67 | ||||
chr2:37084275-37084559 | Common:3; Rare:106 | ||||
chr2:37231412-37231726 | Common:5; Rare:156; Clinvar (benign):4 | ||||
chr2:37324695-37324894 | Common:1; Rare:80 | ||||
chr2:37672881-37672902 | Rare:4 | ||||
chr2:38076143-38076276 | Rare:32 | ||||
chr2:38751354-38751628 | Common:4; Rare:122 | ||||
chr2:38875886-38876055 | Common:1; Rare:63 | ||||
chr2:39437065-39437469 | Common:4; Rare:146 | ||||
chr2:40511768-40512018 | Common:1; Rare:46 | ||||
chr2:43595947-43596197 | Common:1; Rare:87 | ||||
chr2:44361483-44362010 | Common:4; Rare:166 | ||||
chr2:46297258-46297437 | Common:2; Rare:62 | ||||
chr2:46543040-46543438 | Rare:108 |