Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91500666-91500934 | Common:2; Rare:84 | ||||
chr1:91501410-91501784 | Common:1; Rare:99 | ||||
chr1:92080209-92080545 | Common:2; Rare:77 | ||||
chr1:92298898-92299089 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92792408-92792532 | Common:1; Rare:26 | ||||
chr1:92831953-92832147 | Common:1; Rare:96; Clinvar:7; Clinvar (benign):7 | ||||
chr1:92832193-92832337 | Rare:43 | ||||
chr1:92961430-92961613 | Rare:69 | ||||
chr1:93079018-93079507 | Common:4; Rare:173 | ||||
chr1:93079798-93080139 | Common:1; Rare:64 | ||||
chr1:93120247-93120958 | Common:2; Rare:124 | ||||
chr1:93179859-93180020 | Common:1; Rare:44 | ||||
chr1:93180106-93180193 | Rare:31 | ||||
chr1:93180258-93180855 | Common:2; Rare:241 | ||||
chr1:93345610-93346017 | Common:6; Rare:137 |