Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38009163-38009348 | Rare:33 | ||||
chr1:38859686-38860033 | Rare:134 | ||||
chr1:38873301-38873554 | Common:3; Rare:87 | ||||
chr1:38941742-38941895 | Rare:29 | ||||
chr1:39026166-39026398 | Common:1; Rare:58 | ||||
chr1:39204557-39204910 | Rare:56 | ||||
chr1:39204915-39205034 | Rare:28 | ||||
chr1:39284163-39284361 | Common:1; Rare:44 | ||||
chr1:39672073-39672207 | Common:2; Rare:46 | ||||
chr1:39738724-39738930 | Common:2; Rare:51 | ||||
chr1:39883380-39883570 | Common:1; Rare:78; Clinvar (pathogenic):1 | ||||
chr1:40040439-40040799 | Common:3; Rare:109 | ||||
chr1:40070739-40070980 | Rare:50 | ||||
chr1:40161231-40161409 | Common:1; Rare:48 | ||||
chr1:40257895-40258332 | Common:4; Rare:129; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 |