Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11037580-11037900 | Common:1; Rare:104; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11594170-11594660 | Common:4; Rare:105 | ||||
chr1:11731710-11732020 | Common:5; Rare:74 | ||||
chr1:11736850-11736979 | Common:5; Rare:34 | ||||
chr1:11908144-11908483 | Common:40; Rare:368 | ||||
chr1:11908856-11909102 | Common:2; Rare:66 | ||||
chr1:11909755-11910187 | Common:20; Rare:228 | ||||
chr1:11928144-11928294 | Rare:33 | ||||
chr1:11929932-11930128 | Common:1; Rare:39 | ||||
chr1:12052082-12052207 | Rare:25 | ||||
chr1:12081883-12082016 | Rare:31 | ||||
chr1:12148320-12148720 | Common:6; Rare:64 | ||||
chr1:12161878-12162091 | Rare:27 | ||||
chr1:12177850-12178270 | Common:2; Rare:76 | ||||
chr1:12231044-12231212 | Common:2; Rare:38 |