Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:108200142-108200429 | Common:8; Rare:88 | ||||
chr1:108692197-108692365 | Common:1; Rare:65 | ||||
chr1:109075948-109076109 | Rare:62 | ||||
chr1:109090646-109090802 | Common:3; Rare:28 | ||||
chr1:109213742-109213984 | Rare:95 | ||||
chr1:109283087-109283273 | Common:1; Rare:42 | ||||
chr1:109426358-109426585 | Common:1; Rare:87 | ||||
chr1:109548485-109548707 | Common:4; Rare:84 | ||||
chr1:110407592-110407809 | Common:2; Rare:93 | ||||
chr1:111140041-111140272 | Common:2; Rare:81 | ||||
chr1:112395970-112396265 | Common:2; Rare:93 | ||||
chr1:112619109-112619236 | Rare:45 | ||||
chr1:112619642-112619851 | Common:1; Rare:72 | ||||
chr1:112956104-112956437 | Common:4; Rare:132; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073081-113073217 | Common:1; Rare:46 |