Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45499960-45500370 | Common:2; Rare:97; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521798-45522074 | Common:1; Rare:105 | ||||
chr1:45550724-45551135 | Common:3; Rare:99 | ||||
chr1:45567862-45567992 | Common:1; Rare:35 | ||||
chr1:45568235-45568487 | Rare:47 | ||||
chr1:45583906-45584198 | Common:1; Rare:110 | ||||
chr1:45687017-45687214 | Common:2; Rare:61 | ||||
chr1:45688042-45688273 | Common:1; Rare:62 | ||||
chr1:46023104-46023246 | Rare:33 | ||||
chr1:46132117-46132457 | Common:2; Rare:69 | ||||
chr1:46197764-46197954 | Rare:42; Clinvar:3; Clinvar (benign):2 | ||||
chr1:46203200-46203374 | Rare:38 | ||||
chr1:46247347-46247745 | Common:4; Rare:72 | ||||
chr1:46300725-46300968 | Common:1; Rare:34 | ||||
chr1:46302820-46303742 | Common:4; Rare:254 |