Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243850995-243851188 | Rare:73 | ||||
chr1:244048030-244048731 | Common:1; Rare:216 | ||||
chr1:244451686-244451940 | Rare:78 | ||||
chr1:244452035-244452310 | Common:2; Rare:89 | ||||
chr1:244461175-244461613 | Common:3; Rare:144 | ||||
chr1:244461699-244461893 | Rare:46 | ||||
chr1:244652505-244652944 | Common:4; Rare:111 | ||||
chr1:244652947-244653247 | Common:3; Rare:116 | ||||
chr1:244653298-244653353 | Rare:20 | ||||
chr1:244653619-244653697 | Common:1; Rare:24 | ||||
chr1:244653757-244654089 | Common:1; Rare:91 | ||||
chr1:244834731-244835425 | Common:1; Rare:225 | ||||
chr1:244835434-244835790 | Common:5; Rare:140; Clinvar:1; Clinvar (benign):6 | ||||
chr1:244862960-244863301 | Common:4; Rare:137 | ||||
chr1:244863310-244863435 | Common:5; Rare:44 |