Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:219324387-219324549 | Rare:28 | ||||
chr1:219325148-219325294 | Rare:30 | ||||
chr1:219325681-219325895 | Rare:26 | ||||
chr1:219453354-219453569 | Rare:46 | ||||
chr1:220018618-220018844 | Common:1; Rare:30 | ||||
chr1:220102497-220102778 | Rare:62; Clinvar (benign):1 | ||||
chr1:220167317-220167581 | Rare:76; Clinvar:1 | ||||
chr1:220270538-220270752 | Common:2; Rare:33 | ||||
chr1:220271383-220271614 | Common:2; Rare:30 | ||||
chr1:220316910-220317079 | Rare:31 | ||||
chr1:220876649-220877018 | Rare:55 | ||||
chr1:220880005-220880347 | Common:4; Rare:115 | ||||
chr1:221394616-221394702 | Common:1; Rare:12 | ||||
chr1:221443055-221443240 | Common:3; Rare:51 | ||||
chr1:221712610-221712774 | Rare:31 |