Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151790428-151790859 | Common:3; Rare:104 | ||||
chr1:153545605-153546047 | Common:1; Rare:79 | ||||
chr1:153627482-153627893 | Common:2; Rare:92 | ||||
chr1:153633985-153634133 | Common:1; Rare:49 | ||||
chr1:153634303-153634435 | Common:1; Rare:41 | ||||
chr1:153658652-153658739 | Common:1; Rare:30 | ||||
chr1:153678528-153678658 | Common:1; Rare:26 | ||||
chr1:153963497-153963738 | Common:2; Rare:64 | ||||
chr1:153967723-153967954 | Rare:41 | ||||
chr1:153990618-153990799 | Common:2; Rare:76 | ||||
chr1:154183022-154183281 | Rare:84 | ||||
chr1:154220515-154220984 | Common:1; Rare:157 | ||||
chr1:154221249-154221361 | Rare:29 | ||||
chr1:154272420-154272676 | Common:4; Rare:56; Clinvar:1; Clinvar (benign):3 | ||||
chr1:154974306-154974730 | Rare:107 |