Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:2392255-2392655 | Common:1; Rare:144 | ||||
chr1:2412200-2412430 | Rare:63; Clinvar:1 | ||||
chr1:2412461-2412879 | Common:8; Rare:817; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
chr1:2412880-2413130 | Rare:92 | ||||
chr1:2414187-2414587 | Common:2; Rare:110 | ||||
chr1:2526076-2526891 | Common:20; Rare:798 | ||||
chr1:2556220-2557053 | Common:8; Rare:490; Clinvar:1 | ||||
chr1:2556960-2557310 | Common:6; Rare:128 | ||||
chr1:2560590-2561110 | Common:3; Rare:302; Clinvar:2 | ||||
chr1:2585730-2586137 | Common:1; Rare:242 | ||||
chr1:2586267-2586870 | Common:16; Rare:619 | ||||
chr1:2586776-2587328 | Common:6; Rare:194 | ||||
chr1:3454120-3454684 | Rare:260 | ||||
chr1:3454881-3455281 | Common:2; Rare:95 | ||||
chr1:3471870-3472200 | Common:2; Rare:82 |