Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94326335-94326735 | Rare:116 | ||||
chr1:94327279-94327680 | Common:2; Rare:70 | ||||
chr1:94330060-94330228 | Rare:28 | ||||
chr1:94579987-94580100 | Rare:12 | ||||
chr1:94606509-94606937 | Common:4; Rare:98 | ||||
chr1:94621399-94621799 | Common:5; Rare:109 | ||||
chr1:94622696-94623096 | Common:3; Rare:112 | ||||
chr1:94654163-94654285 | Common:1; Rare:19 | ||||
chr1:94713750-94714130 | Rare:78 | ||||
chr1:94802102-94802227 | Rare:23 | ||||
chr1:94854410-94854680 | Rare:58 | ||||
chr1:94864100-94864238 | Rare:24 | ||||
chr1:97138377-97138549 | Common:1; Rare:30 | ||||
chr1:97193010-97193300 | Rare:81; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr1:97277640-97278250 | Common:3; Rare:106 |