Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155008490-155008837 | Rare:65 | ||||
chr1:155010639-155010932 | Rare:54 | ||||
chr1:155011115-155011221 | Common:1; Rare:22 | ||||
chr1:155313481-155313505 | Rare:4 | ||||
chr1:155942885-155942954 | Rare:5 | ||||
chr1:155983382-155983518 | Rare:16 | ||||
chr1:156130311-156130771 | Common:3; Rare:112; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
chr1:156138746-156138863 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):2 | ||||
chr1:156282207-156282264 | Rare:7 | ||||
chr1:156661433-156661631 | Rare:39 | ||||
chr1:156749769-156750019 | Common:2; Rare:46 | ||||
chr1:159929770-159929875 | Rare:44 | ||||
chr1:160295839-160296015 | Common:1; Rare:31 | ||||
chr1:161399626-161399799 | Common:5; Rare:125 | ||||
chr1:161530880-161531118 | Common:5; Rare:98 |