Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:32039744-32039851 | Rare:34 | ||||
chr2:32165701-32165898 | Common:1; Rare:78 | ||||
chr2:32277788-32277977 | Common:1; Rare:47 | ||||
chr2:32628033-32628119 | Rare:25 | ||||
chr2:37084293-37084561 | Common:3; Rare:102 | ||||
chr2:37231519-37231703 | Common:5; Rare:102; Clinvar (benign):3 | ||||
chr2:37344666-37344738 | Common:1; Rare:27 | ||||
chr2:38076149-38076416 | Common:2; Rare:62 | ||||
chr2:38602895-38603187 | Common:4; Rare:114 | ||||
chr2:38875886-38876055 | Common:1; Rare:63 | ||||
chr2:39437078-39437453 | Common:4; Rare:134 | ||||
chr2:43226602-43226856 | Common:1; Rare:100 | ||||
chr2:44361483-44362005 | Common:3; Rare:165 | ||||
chr2:46297650-46297796 | Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
chr2:46617000-46617252 | Common:6; Rare:101 |