Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111989161-111989217 | Rare:16 | ||||
chr1:112395997-112396272 | Common:1; Rare:87 | ||||
chr1:112619099-112619244 | Rare:52 | ||||
chr1:112619642-112619844 | Common:1; Rare:71 | ||||
chr1:112707088-112707253 | Rare:59 | ||||
chr1:112956173-112956473 | Common:5; Rare:129; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073081-113073257 | Common:1; Rare:70 | ||||
chr1:113390419-113390531 | Common:1; Rare:32 | ||||
chr1:113759510-113759572 | Common:1; Rare:17 | ||||
chr1:113812273-113812579 | Common:2; Rare:121 | ||||
chr1:113887562-113887663 | Common:1; Rare:15 | ||||
chr1:113904831-113905407 | Common:7; Rare:173; Clinvar (benign):1 | ||||
chr1:113929270-113929324 | Common:1; Rare:12 | ||||
chr1:114152914-114153053 | Common:2; Rare:40 | ||||
chr1:114581528-114581818 | Common:1; Rare:129 |