Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109548505-109548677 | Common:4; Rare:64 | ||||
chr1:109656016-109656371 | Common:3; Rare:94 | ||||
chr1:110339142-110339452 | Common:1; Rare:86 | ||||
chr1:110407624-110407792 | Common:2; Rare:76 | ||||
chr1:111139377-111139512 | Common:1; Rare:31 | ||||
chr1:111140069-111140263 | Common:1; Rare:68 | ||||
chr1:111619675-111619846 | Common:1; Rare:70 | ||||
chr1:111739361-111739579 | Common:3; Rare:59 | ||||
chr1:112619109-112619199 | Rare:32 | ||||
chr1:112619642-112619846 | Common:1; Rare:71 | ||||
chr1:112707085-112707279 | Rare:67 | ||||
chr1:112956180-112956433 | Common:4; Rare:114; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073100-113073202 | Rare:39 | ||||
chr1:113904797-113905148 | Common:2; Rare:97; Clinvar (benign):1 | ||||
chr1:116909823-116910125 | Rare:86 |