Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117929612-117929795 | Rare:46 | ||||
chr1:119140578-119140774 | Common:1; Rare:74; Clinvar (pathogenic):1 | ||||
chr1:145823895-145824225 | Rare:116 | ||||
chr1:145918663-145919013 | Common:2; Rare:84; Clinvar:1 | ||||
chr1:145927478-145927612 | Rare:31 | ||||
chr1:145964582-145964731 | Rare:34 | ||||
chr1:147172447-147172745 | Common:1; Rare:77 | ||||
chr1:149886675-149886926 | Rare:72 | ||||
chr1:149927764-149927910 | Common:1; Rare:57; Clinvar (benign):4 | ||||
chr1:150067699-150067840 | Rare:39 | ||||
chr1:150629555-150629853 | Common:1; Rare:62 | ||||
chr1:150806937-150806984 | Rare:9 | ||||
chr1:150974666-150974957 | Common:2; Rare:96 | ||||
chr1:151165856-151166157 | Common:3; Rare:85 | ||||
chr1:151254612-151254829 | Rare:55 |