Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19596744-19597113 | Common:3; Rare:138 | ||||
chr1:19643612-19643763 | Common:1; Rare:21 | ||||
chr1:19799864-19800004 | Common:2; Rare:51 | ||||
chr1:20185800-20186138 | Common:1; Rare:97 | ||||
chr1:20486196-20486441 | Rare:55 | ||||
chr1:20508057-20508194 | Common:2; Rare:49 | ||||
chr1:20661338-20661709 | Common:3; Rare:133; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786595-20786861 | Rare:101 | ||||
chr1:21176860-21177015 | Rare:42 | ||||
chr1:21345463-21345655 | Common:2; Rare:75 | ||||
chr1:21782945-21783272 | Common:2; Rare:113 | ||||
chr1:22052544-22052747 | Common:2; Rare:68 | ||||
chr1:23019327-23019510 | Rare:57 | ||||
chr1:23081353-23081537 | Rare:37 | ||||
chr1:23344214-23344585 | Common:2; Rare:126 |