Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207321671-207321779 | Rare:28 | ||||
chr1:207751946-207752275 | Common:2; Rare:102; Clinvar:1 | ||||
chr1:209652403-209652610 | Common:2; Rare:46; Clinvar:1 | ||||
chr1:209675281-209675431 | Common:1; Rare:38 | ||||
chr1:209784525-209784755 | Common:1; Rare:77 | ||||
chr1:209806009-209806315 | Common:5; Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
chr1:209827853-209828036 | Common:1; Rare:45 | ||||
chr1:212035510-212035801 | Common:2; Rare:77 | ||||
chr1:212608153-212608763 | Common:4; Rare:143 | ||||
chr1:212791755-212791964 | Common:4; Rare:95 | ||||
chr1:213015438-213015628 | Rare:57 | ||||
chr1:213051185-213051351 | Rare:55 | ||||
chr1:214281021-214281257 | Common:2; Rare:103 | ||||
chr1:214551623-214551939 | Common:2; Rare:106 | ||||
chr1:217631020-217631385 | Common:3; Rare:104 |