Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:185157434-185157499 | Common:1; Rare:18 | ||||
chr1:185317231-185317468 | Common:1; Rare:70 | ||||
chr1:186375111-186375470 | Rare:101 | ||||
chr1:186375667-186375900 | Common:1; Rare:61 | ||||
chr1:193059330-193059665 | Rare:155 | ||||
chr1:193105367-193105543 | Common:3; Rare:78 | ||||
chr1:193186578-193186687 | Rare:17 | ||||
chr1:201112389-201112681 | Common:3; Rare:69; Clinvar:2; Clinvar (benign):7 | ||||
chr1:201377632-201377979 | Common:4; Rare:74; Clinvar (benign):2 | ||||
chr1:201421671-201421869 | Rare:37 | ||||
chr1:201429810-201429996 | Rare:33 | ||||
chr1:201946452-201946793 | Common:2; Rare:55 | ||||
chr1:202341911-202342193 | Common:1; Rare:74 | ||||
chr1:202539333-202539503 | Rare:27 | ||||
chr1:203007249-203007448 | Common:2; Rare:80 |