Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109090632-109090838 | Common:4; Rare:41 | ||||
chr1:109112724-109112895 | Rare:41 | ||||
chr1:109113853-109114116 | Common:3; Rare:57 | ||||
chr1:109548485-109548686 | Common:4; Rare:74 | ||||
chr1:110339154-110339462 | Common:1; Rare:89 | ||||
chr1:110407628-110407809 | Common:2; Rare:83 | ||||
chr1:111139792-111139889 | Rare:14 | ||||
chr1:111140049-111140286 | Common:2; Rare:79 | ||||
chr1:111346526-111346670 | Common:1; Rare:39 | ||||
chr1:112395954-112396265 | Common:2; Rare:101 | ||||
chr1:112619109-112619199 | Rare:32 | ||||
chr1:112619643-112619871 | Common:1; Rare:82 | ||||
chr1:112956188-112956433 | Common:4; Rare:112; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073085-113073221 | Common:1; Rare:46 | ||||
chr1:113812273-113812397 | Common:2; Rare:58 |