Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:205749964-205750068 | Common:3; Rare:44 | ||||
chr1:205750166-205750410 | Common:3; Rare:54 | ||||
chr1:205813068-205813413 | Common:3; Rare:143 | ||||
chr1:206612356-206612708 | Common:6; Rare:106 | ||||
chr1:206635412-206635586 | Common:1; Rare:51 | ||||
chr1:206909510-206909664 | Common:3; Rare:37 | ||||
chr1:207050935-207051091 | Common:1; Rare:75 | ||||
chr1:207052941-207053295 | Common:1; Rare:90 | ||||
chr1:207321566-207321811 | Rare:62 | ||||
chr1:207751856-207752296 | Common:2; Rare:147; Clinvar:1 | ||||
chr1:208244272-208244531 | Common:1; Rare:79 | ||||
chr1:209675259-209675435 | Common:1; Rare:43 | ||||
chr1:209784521-209784704 | Rare:59 | ||||
chr1:209827814-209828083 | Common:2; Rare:71 | ||||
chr1:209937970-209938273 | Common:3; Rare:104; Clinvar (pathogenic):1 |