Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19596835-19597102 | Common:2; Rare:113 | ||||
chr1:20486198-20486376 | Rare:40 | ||||
chr1:20786595-20786838 | Rare:91 | ||||
chr1:21176872-21177092 | Rare:52 | ||||
chr1:21345454-21345798 | Common:3; Rare:110 | ||||
chr1:21440063-21440179 | Common:1; Rare:27 | ||||
chr1:21783086-21783293 | Common:2; Rare:75 | ||||
chr1:23019327-23019468 | Rare:35 | ||||
chr1:23177698-23177774 | Rare:15 | ||||
chr1:23424624-23424897 | Common:1; Rare:80 | ||||
chr1:23559173-23559317 | Rare:63 | ||||
chr1:23559335-23559643 | Common:1; Rare:134 | ||||
chr1:23691590-23691826 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23778281-23778603 | Common:10; Rare:130 | ||||
chr1:23800741-23800959 | Common:1; Rare:75 |