Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:103525911-103525985 | Rare:18 | ||||
chr1:107056657-107056709 | Rare:26 | ||||
chr1:108200159-108200391 | Common:7; Rare:69 | ||||
chr1:109090649-109090788 | Common:3; Rare:24 | ||||
chr1:109213730-109213995 | Rare:103 | ||||
chr1:109283104-109283357 | Common:2; Rare:61 | ||||
chr1:109548507-109548653 | Common:2; Rare:52 | ||||
chr1:110339146-110339447 | Common:1; Rare:84 | ||||
chr1:110407632-110407820 | Common:3; Rare:87 | ||||
chr1:111140069-111140263 | Common:1; Rare:68 | ||||
chr1:112619099-112619199 | Rare:36 | ||||
chr1:112619734-112619860 | Common:1; Rare:49 | ||||
chr1:112956175-112956393 | Common:4; Rare:94; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073095-113073247 | Common:1; Rare:58 | ||||
chr1:113905025-113905344 | Common:3; Rare:86 |