Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:41621046-41621414 | Common:7; Rare:130 | ||||
chr22:41832876-41833145 | Common:3; Rare:87 | ||||
chr22:41947064-41947236 | Common:1; Rare:63 | ||||
chr22:42090748-42091004 | Common:1; Rare:89 | ||||
chr22:42614846-42615244 | Common:3; Rare:163 | ||||
chr22:43143329-43143445 | Common:2; Rare:41 | ||||
chr22:44668458-44668788 | Common:5; Rare:124 | ||||
chr22:45163792-45163922 | Common:2; Rare:45 | ||||
chr22:46250257-46250377 | Common:2; Rare:33 | ||||
chr22:46762526-46762676 | Common:3; Rare:51 | ||||
chr22:49918286-49918733 | Common:4; Rare:160; Clinvar (benign):3 | ||||
chr22:50278286-50278516 | Rare:70 | ||||
chr22:50525532-50525728 | Common:5; Rare:98; Clinvar:3; Clinvar (benign):2 | ||||
chr22:50582401-50582455 | Rare:30 | ||||
chr22:50582784-50583136 | Common:7; Rare:114; Clinvar:2; Clinvar (benign):3 |