Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:12616409-12616593 | Common:2; Rare:37 | ||||
chr1:15152320-15152566 | Rare:40 | ||||
chr1:15153608-15153783 | Common:1; Rare:48 | ||||
chr1:15584862-15585166 | Common:5; Rare:89 | ||||
chr1:15729552-15729881 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
chr1:15736025-15736361 | Common:3; Rare:61 | ||||
chr1:15736895-15737000 | Rare:17 | ||||
chr1:15742378-15742574 | Common:3; Rare:55 | ||||
chr1:15756542-15756728 | Rare:50 | ||||
chr1:15758740-15758811 | Common:1; Rare:15 | ||||
chr1:15847500-15847836 | Rare:121 | ||||
chr1:15946199-15946426 | Rare:61 | ||||
chr1:16352291-16352604 | Common:3; Rare:145 | ||||
chr1:16440783-16440852 | Common:1; Rare:26 | ||||
chr1:17439669-17439871 | Rare:64 |