Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:32857116-32857384 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
chr22:36282747-36282873 | Common:3; Rare:38; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr22:36288746-36289301 | Common:2; Rare:167; Clinvar:5; Clinvar (benign):10 | ||||
chr22:36323228-36323270 | Common:1; Rare:4 | ||||
chr22:36455076-36455349 | Common:4; Rare:86 | ||||
chr22:37631735-37632050 | Common:2; Rare:79 | ||||
chr22:37806228-37806537 | Common:3; Rare:56 | ||||
chr22:38204710-38204762 | Common:1; Rare:8 | ||||
chr22:39521546-39521846 | Common:1; Rare:140 | ||||
chr22:41092883-41092920 | Rare:11 | ||||
chr22:41529276-41529489 | Rare:54 | ||||
chr22:42601041-42601229 | Common:1; Rare:44 | ||||
chr22:45570183-45570279 | Common:2; Rare:12 | ||||
chr22:45626442-45626481 | Common:1; Rare:7 | ||||
chr22:46069842-46070067 | Rare:48 |