Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:203627951-203628043 | Rare:13 | ||||
chr1:203672256-203672584 | Common:4; Rare:65 | ||||
chr1:203771850-203772045 | Common:1; Rare:38 | ||||
chr1:206890769-206891066 | Common:5; Rare:56 | ||||
chr1:206905457-206905636 | Rare:32 | ||||
chr1:207024993-207025145 | Common:2; Rare:70 | ||||
chr1:209653102-209653293 | Common:1; Rare:34 | ||||
chr1:211382661-211382865 | Common:1; Rare:83 | ||||
chr1:218345228-218345426 | Common:1; Rare:32; Clinvar (benign):1 | ||||
chr1:220300519-220300710 | Common:1; Rare:42 | ||||
chr1:221711129-221711252 | Common:1; Rare:28 | ||||
chr1:222044287-222044334 | Common:1; Rare:7 | ||||
chr1:222814807-222815089 | Common:7; Rare:92 | ||||
chr1:223027864-223027944 | Common:2; Rare:22 | ||||
chr1:223750747-223750973 | Common:1; Rare:61 |