Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117367297-117367538 | Common:5; Rare:88 | ||||
chr1:117367713-117367813 | Rare:22 | ||||
chr1:117368333-117368445 | Rare:32 | ||||
chr1:117929566-117929871 | Common:4; Rare:91 | ||||
chr1:119140597-119140771 | Common:1; Rare:61; Clinvar (pathogenic):1 | ||||
chr1:119648138-119648351 | Common:3; Rare:77 | ||||
chr1:145773348-145773492 | Rare:33 | ||||
chr1:145773498-145773782 | Common:2; Rare:39 | ||||
chr1:145823936-145824297 | Rare:127 | ||||
chr1:145845451-145845636 | Common:3; Rare:39 | ||||
chr1:145858983-145859195 | Rare:61 | ||||
chr1:145859681-145859941 | Common:2; Rare:75 | ||||
chr1:145918636-145919057 | Common:2; Rare:102; Clinvar:2 | ||||
chr1:145927477-145927655 | Rare:44 | ||||
chr1:145957927-145958086 | Rare:43 |