Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234373623-234373775 | Rare:59; Clinvar (benign):3 | ||||
chr1:235128801-235129048 | Rare:96 | ||||
chr1:235327827-235327846 | Rare:5 | ||||
chr1:235328151-235328409 | Common:2; Rare:74 | ||||
chr1:235328472-235328584 | Common:1; Rare:34 | ||||
chr1:236065062-236065344 | Common:2; Rare:110; Clinvar (pathogenic):1 | ||||
chr1:241848123-241848234 | Common:1; Rare:20 | ||||
chr1:243255053-243255422 | Common:1; Rare:84 | ||||
chr1:243255776-243256117 | Rare:96; Clinvar:4 | ||||
chr1:244451884-244452127 | Common:1; Rare:90 | ||||
chr1:244835134-244835333 | Rare:81 | ||||
chr1:244864309-244864677 | Rare:136 | ||||
chr1:246566195-246566579 | Common:1; Rare:127 | ||||
chr1:247104301-247104561 | Common:2; Rare:79 | ||||
chr1:248858925-248859165 | Rare:93 |