Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:51280694-51280762 | Common:2; Rare:8 | ||||
chr1:51518097-51518305 | Rare:47 | ||||
chr1:51797590-51797841 | Rare:46 | ||||
chr1:51798381-51798473 | Common:1; Rare:29 | ||||
chr1:52414392-52414620 | Common:4; Rare:44 | ||||
chr1:52917144-52917431 | Common:1; Rare:60 | ||||
chr1:52918858-52918912 | Rare:8 | ||||
chr1:54224966-54225246 | Common:3; Rare:64 | ||||
chr1:54241472-54241774 | Common:2; Rare:80 | ||||
chr1:58575648-58575866 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
chr1:58575912-58576179 | Common:4; Rare:53; Clinvar:2; Clinvar (benign):5 | ||||
chr1:58576256-58577142 | Common:5; Rare:349; Clinvar:4; Clinvar (benign):5 | ||||
chr1:58577249-58577259 | Rare:1 | ||||
chr1:58618351-58618384 | Common:1; Rare:5 | ||||
chr1:58782079-58782443 | Common:1; Rare:88; Clinvar:1 |