Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11805831-11806276 | Common:2; Rare:123; Clinvar:2 | ||||
chr1:11934469-11934784 | Common:6; Rare:99; Clinvar:6; Clinvar (benign):1 | ||||
chr1:12019201-12019528 | Common:5; Rare:115 | ||||
chr1:12618191-12618475 | Common:2; Rare:60 | ||||
chr1:13749052-13749451 | Common:2; Rare:129 | ||||
chr1:14598391-14598691 | Common:1; Rare:90 | ||||
chr1:14598737-14598841 | Common:1; Rare:31 | ||||
chr1:15152457-15152639 | Rare:27 | ||||
chr1:15409803-15409912 | Rare:34 | ||||
chr1:15526553-15526905 | Common:2; Rare:112 | ||||
chr1:15758597-15758822 | Common:1; Rare:53 | ||||
chr1:16017403-16017621 | Common:1; Rare:42 | ||||
chr1:16017644-16017686 | Rare:7 | ||||
chr1:16017763-16018297 | Common:9; Rare:183 | ||||
chr1:16048555-16048873 | Common:6; Rare:98; Clinvar (benign):2 |