Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21290794-21290925 | Common:2; Rare:17 | ||||
chr1:21294411-21294461 | Rare:4 | ||||
chr1:21783086-21783304 | Common:3; Rare:81 | ||||
chr1:22451797-22451885 | Rare:36 | ||||
chr1:23019259-23019532 | Rare:85 | ||||
chr1:23559427-23559643 | Common:1; Rare:93 | ||||
chr1:23627223-23627475 | Rare:65 | ||||
chr1:23778275-23778431 | Common:6; Rare:82 | ||||
chr1:23791062-23791245 | Rare:57 | ||||
chr1:23800750-23800962 | Common:1; Rare:74 | ||||
chr1:23825408-23825534 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959065-23959378 | Common:3; Rare:67 | ||||
chr1:23959607-23959950 | Common:2; Rare:87 | ||||
chr1:23980264-23980504 | Rare:76 | ||||
chr1:24502739-24502845 | Rare:33 |