Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113979208-113979522 | Common:1; Rare:125 | ||||
chr1:114510253-114510840 | Common:1; Rare:206 | ||||
chr1:114510780-114511682 | Common:25; Rare:823 | ||||
chr1:114581539-114581959 | Common:3; Rare:437 | ||||
chr1:114669961-114670323 | Common:3; Rare:281 | ||||
chr1:114716612-114716985 | Common:6; Rare:311; Clinvar:14; Clinvar (benign):7 | ||||
chr1:114757211-114757743 | Common:1; Rare:262 | ||||
chr1:114757864-114758303 | Common:9; Rare:249 | ||||
chr1:114758533-114759140 | Rare:127 | ||||
chr1:114780384-114780902 | Common:4; Rare:389 | ||||
chr1:115089446-115089688 | Common:3; Rare:87 | ||||
chr1:115641666-115642144 | Common:11; Rare:331; Clinvar:8; Clinvar (benign):6 | ||||
chr1:115642413-115642738 | Common:4; Rare:141 | ||||
chr1:115642770-115643390 | Common:7; Rare:124 | ||||
chr1:115671293-115671819 | Common:7; Rare:134 |