Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:108692221-108692340 | Common:1; Rare:36 | ||||
chr1:109075943-109076067 | Rare:50 | ||||
chr1:109090646-109090844 | Common:3; Rare:42 | ||||
chr1:109283104-109283305 | Common:1; Rare:49 | ||||
chr1:109426395-109426630 | Common:2; Rare:79 | ||||
chr1:109548505-109548675 | Common:4; Rare:63 | ||||
chr1:110339133-110339480 | Common:1; Rare:105 | ||||
chr1:110407632-110407774 | Common:2; Rare:64 | ||||
chr1:111140046-111140286 | Common:2; Rare:82 | ||||
chr1:111346348-111346642 | Common:1; Rare:69 | ||||
chr1:112395908-112396257 | Common:2; Rare:111 | ||||
chr1:112619096-112619212 | Rare:39 | ||||
chr1:112619605-112619851 | Common:1; Rare:81 | ||||
chr1:112956145-112956410 | Common:4; Rare:113; Clinvar:10; Clinvar (benign):3 | ||||
chr1:114780564-114780805 | Common:1; Rare:91 |