Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:213015844-213015927 | Rare:25 | ||||
chr1:214280997-214281246 | Common:2; Rare:104 | ||||
chr1:214603017-214603321 | Common:3; Rare:85 | ||||
chr1:217631020-217631366 | Common:2; Rare:93 | ||||
chr1:218285178-218285350 | Common:2; Rare:83 | ||||
chr1:218345956-218346098 | Common:5; Rare:48; Clinvar:7; Clinvar (benign):3 | ||||
chr1:218346892-218346943 | Rare:12; Clinvar:5; Clinvar (pathogenic):1 | ||||
chr1:219173808-219173893 | Rare:47 | ||||
chr1:222589912-222589970 | Rare:10 | ||||
chr1:222644159-222644387 | Common:1; Rare:65 | ||||
chr1:222712437-222712864 | Common:3; Rare:149 | ||||
chr1:224113982-224114129 | Common:1; Rare:53 | ||||
chr1:224183038-224183314 | Common:3; Rare:114 | ||||
chr1:224330131-224330438 | Common:6; Rare:93 | ||||
chr1:224616218-224616253 | Common:1; Rare:8 |