Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236604486-236604628 | Common:4; Rare:41 | ||||
chr1:239386462-239386636 | Rare:28 | ||||
chr1:241519674-241519963 | Common:2; Rare:94; Clinvar:11; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr1:241848085-241848255 | Common:2; Rare:34 | ||||
chr1:243255040-243255433 | Common:1; Rare:96 | ||||
chr1:243255752-243256107 | Rare:94; Clinvar:4 | ||||
chr1:244051128-244051364 | Rare:27 | ||||
chr1:244451884-244452166 | Common:1; Rare:100 | ||||
chr1:244835115-244835333 | Rare:85 | ||||
chr1:244835562-244835747 | Common:2; Rare:82; Clinvar (benign):5 | ||||
chr1:244864213-244864669 | Rare:156; Clinvar:1; Clinvar (benign):1 | ||||
chr1:246566209-246566515 | Common:1; Rare:102 | ||||
chr1:246724231-246724432 | Common:2; Rare:79 | ||||
chr1:247078760-247078902 | Rare:38 | ||||
chr1:247104311-247104561 | Common:2; Rare:77 |