Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113391440-113391517 | Common:1; Rare:20 | ||||
chr1:113759442-113759673 | Common:3; Rare:70 | ||||
chr1:113759873-113760020 | Rare:24 | ||||
chr1:113811773-113812030 | Rare:91 | ||||
chr1:113812193-113812693 | Common:3; Rare:196 | ||||
chr1:113904566-113904706 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
chr1:113904850-113905455 | Common:7; Rare:180; Clinvar (benign):1 | ||||
chr1:113905660-113905816 | Common:1; Rare:66; Clinvar:3 | ||||
chr1:113928968-113929141 | Rare:35 | ||||
chr1:113929230-113929379 | Common:1; Rare:40 | ||||
chr1:113929433-113929734 | Common:2; Rare:92 | ||||
chr1:113930245-113930306 | Rare:18 | ||||
chr1:113979321-113979508 | Rare:50 | ||||
chr1:114511044-114511430 | Common:4; Rare:159 | ||||
chr1:114511432-114511611 | Common:1; Rare:44 |