Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:201317187-201317407 | Common:2; Rare:45 | ||||
chr1:201317419-201317942 | Common:4; Rare:146; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:201320059-201320397 | Common:1; Rare:111; Clinvar:3 | ||||
chr1:201320626-201320861 | Common:4; Rare:55 | ||||
chr1:201323272-201323562 | Common:3; Rare:57 | ||||
chr1:201325471-201325962 | Common:3; Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
chr1:201327004-201327335 | Common:4; Rare:54 | ||||
chr1:202810753-202810982 | Common:1; Rare:75 | ||||
chr1:203306504-203306730 | Common:1; Rare:34 | ||||
chr1:204410821-204410906 | Rare:29 | ||||
chr1:205843766-205843865 | Common:1; Rare:20 | ||||
chr1:206306562-206306620 | Rare:9 | ||||
chr1:207024941-207025291 | Common:4; Rare:125 | ||||
chr1:207816717-207817022 | Rare:55 | ||||
chr1:207866779-207867098 | Common:1; Rare:56 |