Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113905018-113905390 | Common:5; Rare:106 | ||||
chr1:114152920-114153033 | Common:2; Rare:33 | ||||
chr1:114670047-114670178 | Rare:40 | ||||
chr1:116373109-116373343 | Rare:78 | ||||
chr1:117060072-117060341 | Common:6; Rare:61 | ||||
chr1:117929599-117929800 | Common:1; Rare:55 | ||||
chr1:118185157-118185316 | Rare:43 | ||||
chr1:119140640-119140767 | Rare:38 | ||||
chr1:120176385-120176598 | Rare:49 | ||||
chr1:145823895-145824268 | Rare:134 | ||||
chr1:145918695-145918987 | Common:2; Rare:55 | ||||
chr1:145927431-145927587 | Common:1; Rare:43; Clinvar (pathogenic):1 | ||||
chr1:145964396-145964754 | Rare:73 | ||||
chr1:145996488-145996862 | Common:1; Rare:152 | ||||
chr1:147172427-147172830 | Common:1; Rare:104 |