Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:213015418-213015628 | Rare:58 | ||||
chr1:213987701-213987977 | Rare:51 | ||||
chr1:214280935-214281273 | Common:3; Rare:140 | ||||
chr1:214551560-214551922 | Common:2; Rare:117 | ||||
chr1:215567158-215567175 | Rare:2 | ||||
chr1:215567253-215567773 | Common:1; Rare:163 | ||||
chr1:216723247-216723543 | Rare:79 | ||||
chr1:217078203-217078488 | Common:1; Rare:44 | ||||
chr1:217089616-217089743 | Rare:34 | ||||
chr1:217630928-217631379 | Common:3; Rare:131 | ||||
chr1:218285211-218285452 | Common:3; Rare:99 | ||||
chr1:218346471-218346938 | Common:1; Rare:114; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:219173766-219173907 | Common:1; Rare:77 | ||||
chr1:219174157-219174182 | Rare:5 | ||||
chr1:219174776-219174985 | Rare:33 |