Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114780568-114780787 | Common:1; Rare:84 | ||||
chr1:115089455-115089551 | Rare:40 | ||||
chr1:116373930-116374085 | Common:1; Rare:51 | ||||
chr1:116400660-116400913 | Common:1; Rare:56; Clinvar (pathogenic):1 | ||||
chr1:116570918-116571197 | Common:3; Rare:80 | ||||
chr1:116754351-116754483 | Rare:37 | ||||
chr1:117060066-117060360 | Common:6; Rare:76 | ||||
chr1:117121727-117121958 | Common:1; Rare:62 | ||||
chr1:117367323-117367542 | Common:5; Rare:73 | ||||
chr1:117367634-117367723 | Rare:18 | ||||
chr1:117605783-117606071 | Rare:86 | ||||
chr1:117929546-117929806 | Common:4; Rare:77 | ||||
chr1:119140632-119140776 | Common:1; Rare:48 | ||||
chr1:119648136-119648350 | Common:3; Rare:77 | ||||
chr1:121087080-121087386 | Rare:67 |