Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236604464-236604672 | Common:5; Rare:61 | ||||
chr1:243255169-243255358 | Common:1; Rare:37 | ||||
chr1:243255776-243256128 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244451851-244452027 | Rare:53 | ||||
chr1:244461256-244461332 | Common:1; Rare:19 | ||||
chr1:244835016-244835333 | Rare:118 | ||||
chr1:244835575-244835747 | Common:2; Rare:77; Clinvar (benign):5 | ||||
chr1:244862937-244863273 | Common:4; Rare:131 | ||||
chr1:244864360-244864686 | Rare:126 | ||||
chr1:244969763-244969822 | Rare:17 | ||||
chr1:244970021-244970417 | Common:5; Rare:170 | ||||
chr1:246507229-246507359 | Common:1; Rare:56 | ||||
chr1:246566160-246566596 | Common:3; Rare:147 | ||||
chr1:247171992-247172064 | Common:1; Rare:10 | ||||
chr1:248826264-248826354 | Rare:31 |