Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:110407364-110407409 | Rare:15 | ||||
chr1:110407616-110407809 | Common:2; Rare:88 | ||||
chr1:111139340-111139501 | Common:1; Rare:36 | ||||
chr1:111140036-111140296 | Common:2; Rare:90 | ||||
chr1:111739360-111739561 | Common:3; Rare:51 | ||||
chr1:112396009-112396272 | Common:1; Rare:82 | ||||
chr1:112619099-112619236 | Rare:49 | ||||
chr1:112619642-112619857 | Common:1; Rare:76 | ||||
chr1:112956190-112956437 | Common:4; Rare:112; Clinvar:8; Clinvar (benign):3 | ||||
chr1:113073095-113073221 | Common:1; Rare:45 | ||||
chr1:113812234-113812579 | Common:2; Rare:140 | ||||
chr1:113905016-113905402 | Common:5; Rare:109 | ||||
chr1:114581554-114581818 | Common:1; Rare:123 | ||||
chr1:114716722-114716862 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):1 | ||||
chr1:114757925-114758088 | Common:3; Rare:53 |