Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:42614858-42615246 | Common:3; Rare:161 | ||||
chr22:43089325-43089490 | Common:3; Rare:55 | ||||
chr22:43812214-43812441 | Common:3; Rare:76 | ||||
chr22:43955314-43955560 | Common:3; Rare:73 | ||||
chr22:44024165-44024335 | Common:1; Rare:60 | ||||
chr22:44181204-44181361 | Common:4; Rare:35 | ||||
chr22:44752497-44752613 | Common:3; Rare:47 | ||||
chr22:45163766-45164054 | Common:3; Rare:119 | ||||
chr22:46053786-46053901 | Rare:40 | ||||
chr22:46250268-46250396 | Common:1; Rare:39 | ||||
chr22:46267804-46268037 | Common:1; Rare:65 | ||||
chr22:46335621-46335804 | Common:5; Rare:83; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr22:46762517-46762701 | Common:3; Rare:64 | ||||
chr22:49918293-49918680 | Common:4; Rare:129; Clinvar (benign):3 | ||||
chr22:50244949-50245059 | Common:2; Rare:40 |