Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156003457-156003684 | Rare:39 | ||||
chr1:156052970-156053021 | Common:1; Rare:10 | ||||
chr1:156096738-156096894 | Common:1; Rare:29 | ||||
chr1:156103233-156103273 | Rare:4 | ||||
chr1:156104213-156104394 | Common:1; Rare:36 | ||||
chr1:156115256-156115385 | Rare:25; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:156115572-156115877 | Common:2; Rare:52 | ||||
chr1:156115908-156116059 | Rare:23 | ||||
chr1:156116085-156116407 | Rare:58 | ||||
chr1:156117015-156117249 | Common:2; Rare:29 | ||||
chr1:156118340-156118485 | Common:2; Rare:23 | ||||
chr1:156121150-156121261 | Rare:16 | ||||
chr1:156123760-156124031 | Common:1; Rare:45 | ||||
chr1:156125178-156125453 | Common:1; Rare:36 | ||||
chr1:156127238-156127320 | Rare:16 |