Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9651641-9651765 | Common:3; Rare:29 | ||||
chr1:9687535-9687810 | Common:3; Rare:57 | ||||
chr1:9823963-9824213 | Common:1; Rare:76 | ||||
chr1:9942655-9942899 | Common:1; Rare:40 | ||||
chr1:9943284-9943492 | Common:2; Rare:52 | ||||
chr1:10033372-10033631 | Common:2; Rare:46 | ||||
chr1:10398862-10399103 | Common:2; Rare:90 | ||||
chr1:10796574-10796862 | Common:3; Rare:85 | ||||
chr1:11012620-11012696 | Common:1; Rare:30; Clinvar:3; Clinvar (benign):1 | ||||
chr1:11099749-11099778 | Common:1; Rare:10 | ||||
chr1:11099784-11099957 | Common:2; Rare:71 | ||||
chr1:11189088-11189357 | Common:1; Rare:56 | ||||
chr1:11262496-11262817 | Common:2; Rare:97 | ||||
chr1:11273409-11273503 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11654396-11654498 | Rare:28 |