Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:120095074-120095270 | Common:1; Rare:59 | ||||
chr3:123626935-123626959 | Rare:5; Clinvar:1; Clinvar (benign):1 | ||||
chr3:124631153-124631247 | Common:2; Rare:19 | ||||
chr3:125793471-125793671 | Common:1; Rare:52 | ||||
chr3:125799401-125799531 | Common:4; Rare:53 | ||||
chr3:125810817-125810972 | Rare:35 | ||||
chr3:125830204-125830335 | Common:2; Rare:28 | ||||
chr3:125851962-125851977 | Rare:5 | ||||
chr3:125864416-125864542 | Common:1; Rare:31 | ||||
chr3:125867028-125867172 | Common:1; Rare:37 | ||||
chr3:125867652-125867957 | Common:2; Rare:76 | ||||
chr3:125886067-125886233 | Common:3; Rare:35 | ||||
chr3:125889817-125889939 | Common:1; Rare:39 | ||||
chr3:125916360-125916615 | Common:4; Rare:79 | ||||
chr3:127715073-127715202 | Rare:22 |