Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112619754-112619837 | Common:1; Rare:32 | ||||
chr1:112956185-112956327 | Common:4; Rare:68; Clinvar:7; Clinvar (benign):3 | ||||
chr1:117929618-117929763 | Rare:39 | ||||
chr1:119140632-119140743 | Rare:34 | ||||
chr1:153545569-153545754 | Rare:33 | ||||
chr1:153545795-153545859 | Rare:8 | ||||
chr1:153627642-153627920 | Common:2; Rare:61 | ||||
chr1:153967691-153967914 | Rare:45 | ||||
chr1:154974365-154974698 | Rare:78 | ||||
chr1:155173229-155173388 | Common:2; Rare:72 | ||||
chr1:156054614-156054871 | Common:3; Rare:71 | ||||
chr1:156134954-156135234 | Common:2; Rare:58; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:156338205-156338543 | Common:2; Rare:120 | ||||
chr1:156728417-156728464 | Rare:11 | ||||
chr1:160343218-160343399 | Rare:70 |