Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15409788-15409906 | Rare:38 | ||||
chr1:15526553-15526940 | Common:2; Rare:122 | ||||
chr1:15757736-15757999 | Common:1; Rare:46 | ||||
chr1:15758503-15758831 | Common:1; Rare:67 | ||||
chr1:15976042-15976149 | Common:1; Rare:26 | ||||
chr1:16237137-16237319 | Common:1; Rare:63 | ||||
chr1:16352413-16352575 | Common:2; Rare:90 | ||||
chr1:16440617-16440803 | Common:1; Rare:72 | ||||
chr1:16613480-16613660 | Common:1 | ||||
chr1:17053960-17054362 | Common:3; Rare:124; Clinvar:16; Clinvar (benign):10 | ||||
chr1:17439669-17439937 | Rare:88 | ||||
chr1:17618174-17618424 | Common:3; Rare:56 | ||||
chr1:19210231-19210533 | Common:1; Rare:98 | ||||
chr1:19251494-19251866 | Common:6; Rare:124 | ||||
chr1:19288757-19288865 | Common:1; Rare:35 |