Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149927760-149927875 | Rare:49; Clinvar (benign):3 | ||||
chr1:150629544-150629819 | Rare:52 | ||||
chr1:151165877-151166144 | Common:2; Rare:76 | ||||
chr1:151790467-151790653 | Common:1; Rare:47 | ||||
chr1:153545632-153545860 | Rare:36 | ||||
chr1:153627569-153627879 | Common:2; Rare:69 | ||||
chr1:153963490-153963738 | Common:2; Rare:68 | ||||
chr1:153967732-153967954 | Rare:40 | ||||
chr1:154220521-154220959 | Common:1; Rare:151 | ||||
chr1:154974334-154974695 | Rare:84 | ||||
chr1:155002486-155002669 | Common:1; Rare:14 | ||||
chr1:155051174-155051423 | Common:1; Rare:82 | ||||
chr1:155308486-155309003 | Common:1; Rare:107 | ||||
chr1:155562803-155562964 | Common:1; Rare:91 | ||||
chr1:156134515-156134807 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |