Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:213015621-213015923 | Rare:99 | ||||
chr1:213987614-213988018 | Rare:82 | ||||
chr1:214281069-214281348 | Common:2; Rare:116 | ||||
chr1:214327535-214327721 | Common:1; Rare:41 | ||||
chr1:214330827-214331071 | Rare:62 | ||||
chr1:214551211-214551390 | Common:2; Rare:62 | ||||
chr1:214551397-214551484 | Common:1; Rare:15 | ||||
chr1:215573828-215574116 | Common:1; Rare:57 | ||||
chr1:217630992-217631379 | Common:2; Rare:112 | ||||
chr1:218285185-218285410 | Common:3; Rare:102 | ||||
chr1:218346068-218346554 | Rare:92; Clinvar:2; Clinvar (benign):2 | ||||
chr1:219173745-219174201 | Common:2; Rare:177 | ||||
chr1:219174710-219175000 | Rare:54 | ||||
chr1:220094075-220094445 | Common:4; Rare:136; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:220527977-220528272 | Common:1; Rare:110 |