Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45550667-45551131 | Common:4; Rare:118 | ||||
chr1:45583319-45583582 | Common:3; Rare:66 | ||||
chr1:45583804-45584071 | Common:1; Rare:88 | ||||
chr1:45686477-45686777 | Rare:111 | ||||
chr1:45686975-45687386 | Common:2; Rare:105 | ||||
chr1:45688047-45688243 | Common:1; Rare:56 | ||||
chr1:45750501-45750683 | Rare:54 | ||||
chr1:45750691-45750911 | Common:1; Rare:68 | ||||
chr1:45803385-45803653 | Common:2; Rare:96 | ||||
chr1:46132630-46133440 | Common:3; Rare:232 | ||||
chr1:46183211-46183561 | Common:2; Rare:56 | ||||
chr1:46183614-46183880 | Common:3; Rare:55 | ||||
chr1:46197610-46198030 | Rare:98; Clinvar:8; Clinvar (benign):5 | ||||
chr1:46198402-46198593 | Common:5; Rare:92; Clinvar:1 | ||||
chr1:46220701-46221201 | Common:4; Rare:142 |