Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:605406-605592 | Rare:28 | ||||
chr1:778533-778937 | Common:6; Rare:140 | ||||
chr1:827479-827731 | Common:2; Rare:96 | ||||
chr1:904532-904923 | Common:7; Rare:143 | ||||
chr1:905199-905487 | Common:1; Rare:75 | ||||
chr1:923827-924085 | Common:4; Rare:77 | ||||
chr1:998611-998767 | Common:6; Rare:51 | ||||
chr1:998900-999017 | Common:2; Rare:36 | ||||
chr1:1001888-1001952 | Rare:21 | ||||
chr1:1001954-1001985 | Rare:11 | ||||
chr1:1014491-1014612 | Common:2; Rare:43 | ||||
chr1:1021179-1021376 | Common:1; Rare:47 | ||||
chr1:1040675-1040867 | Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
chr1:1059567-1059741 | Common:1; Rare:75 | ||||
chr1:1069257-1069555 | Rare:112 |