Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10033097-10033251 | Rare:32 | ||||
chr1:10398813-10399124 | Common:2; Rare:123 | ||||
chr1:10431273-10431307 | Rare:9 | ||||
chr1:10472415-10472588 | Rare:55 | ||||
chr1:11059968-11060273 | Common:2; Rare:95 | ||||
chr1:11262496-11262835 | Common:2; Rare:100 | ||||
chr1:11273429-11273519 | Common:1; Rare:31; Clinvar (benign):1 | ||||
chr1:11654323-11654530 | Rare:57 | ||||
chr1:11654532-11654733 | Rare:47 | ||||
chr1:11654757-11654941 | Common:3; Rare:49 | ||||
chr1:11735798-11736234 | Common:3; Rare:115 | ||||
chr1:11805895-11806270 | Common:2; Rare:104; Clinvar:1 | ||||
chr1:11806338-11806466 | Common:2; Rare:35 | ||||
chr1:11926390-11926595 | Common:6; Rare:60 | ||||
chr1:11934780-11934853 | Rare:13; Clinvar:1 |