Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111200118-111200446 | Common:3; Rare:67 | ||||
chr1:111200594-111200667 | Common:1; Rare:12 | ||||
chr1:111473824-111474069 | Common:2; Rare:49 | ||||
chr1:111619816-111619931 | Rare:33 | ||||
chr1:112619594-112619845 | Common:1; Rare:80 | ||||
chr1:112956191-112956297 | Common:4; Rare:48; Clinvar:3; Clinvar (benign):3 | ||||
chr1:113073095-113073221 | Common:1; Rare:45 | ||||
chr1:113871696-113871810 | Rare:21 | ||||
chr1:113904785-113905171 | Common:3; Rare:110; Clinvar (benign):1 | ||||
chr1:113929474-113929651 | Common:1; Rare:48 | ||||
chr1:114581610-114581843 | Rare:92 | ||||
chr1:114716679-114716987 | Common:4; Rare:119; Clinvar:5; Clinvar (benign):2 | ||||
chr1:116570333-116570689 | Common:2; Rare:85 | ||||
chr1:116570980-116571135 | Common:1; Rare:47 | ||||
chr1:117929600-117929800 | Common:1; Rare:54 |