Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:215579921-215580054 | Common:1; Rare:30 | ||||
chr1:218345318-218345601 | Common:3; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
chr1:219442674-219442962 | Common:4; Rare:45 | ||||
chr1:222654293-222654476 | Common:1; Rare:44 | ||||
chr1:222711519-222711595 | Rare:15 | ||||
chr1:223992535-223992812 | Common:4; Rare:105 | ||||
chr1:224375131-224375409 | Common:2; Rare:48 | ||||
chr1:224418322-224418536 | Rare:50 | ||||
chr1:224432419-224432455 | Rare:6 | ||||
chr1:225486742-225486959 | Common:2; Rare:35 | ||||
chr1:225700308-225700764 | Common:4; Rare:72 | ||||
chr1:226083505-226083626 | Common:3; Rare:43 | ||||
chr1:228647690-228647790 | Common:2; Rare:27 | ||||
chr1:229338053-229338335 | Common:1; Rare:47 | ||||
chr1:231335041-231335096 | Rare:8 |