Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92298923-92299076 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92785066-92785384 | Common:6; Rare:102 | ||||
chr1:92831940-92832124 | Common:1; Rare:87; Clinvar:7; Clinvar (benign):6 | ||||
chr1:93079097-93079299 | Common:2; Rare:84 | ||||
chr1:93179812-93179954 | Common:1; Rare:31 | ||||
chr1:93180053-93180548 | Rare:178 | ||||
chr1:93180631-93180762 | Common:2; Rare:62 | ||||
chr1:93345729-93346191 | Common:5; Rare:162 | ||||
chr1:93448007-93448174 | Common:2; Rare:62 | ||||
chr1:93847218-93847279 | Common:1; Rare:15 | ||||
chr1:94418215-94418498 | Common:2; Rare:98 | ||||
chr1:94541624-94542011 | Common:1; Rare:110 | ||||
chr1:94820273-94820440 | Common:2; Rare:48 | ||||
chr1:94903120-94903484 | Common:1; Rare:73 | ||||
chr1:94926854-94927244 | Common:4; Rare:121 |