Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:224434757-224434865 | Rare:30 | ||||
chr1:225427965-225428280 | Common:3; Rare:110; Clinvar:5; Clinvar (benign):3 | ||||
chr1:225652042-225652344 | Rare:62 | ||||
chr1:225653027-225653444 | Common:4; Rare:158 | ||||
chr1:225777538-225777846 | Common:2; Rare:76 | ||||
chr1:225809939-225810136 | Common:4; Rare:48 | ||||
chr1:225924115-225924199 | Rare:40 | ||||
chr1:225924222-225924537 | Common:10; Rare:91 | ||||
chr1:225999305-225999616 | Common:2; Rare:106 | ||||
chr1:226062491-226062725 | Rare:68 | ||||
chr1:226186394-226186786 | Common:1; Rare:112 | ||||
chr1:226309108-226309369 | Common:1; Rare:118 | ||||
chr1:226870523-226870656 | Common:2; Rare:39; Clinvar (benign):2 | ||||
chr1:226939933-226940335 | Rare:136; Clinvar:3 | ||||
chr1:227735217-227735491 | Common:3; Rare:157 |