Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113812231-113812608 | Common:2; Rare:152 | ||||
chr1:113905022-113905434 | Common:5; Rare:114 | ||||
chr1:113979252-113979525 | Common:1; Rare:65 | ||||
chr1:114780549-114780806 | Common:1; Rare:96 | ||||
chr1:115089415-115089610 | Common:2; Rare:76 | ||||
chr1:116909847-116910206 | Common:1; Rare:114 | ||||
chr1:117367323-117367490 | Common:4; Rare:58 | ||||
chr1:117929560-117929802 | Common:3; Rare:70 | ||||
chr1:119140367-119140631 | Common:1; Rare:85; Clinvar (pathogenic):1 | ||||
chr1:119140634-119140735 | Rare:29 | ||||
chr1:119648138-119648350 | Common:3; Rare:77 | ||||
chr1:145823869-145824265 | Rare:137 | ||||
chr1:145918680-145919022 | Common:2; Rare:79 | ||||
chr1:145927374-145927644 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
chr1:145958000-145958202 | Rare:47 |