Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:115841548-115841625 | Common:1; Rare:43 | ||||
chr5:115841826-115842046 | Common:4; Rare:70 | ||||
chr5:116085011-116085055 | Common:1; Rare:24 | ||||
chr5:119070872-119071139 | Common:2; Rare:85 | ||||
chr5:119268626-119268831 | Common:1; Rare:58 | ||||
chr5:119355825-119356045 | Common:3; Rare:55 | ||||
chr5:120464135-120464356 | Common:1; Rare:65 | ||||
chr5:122845323-122845621 | Common:3; Rare:100 | ||||
chr5:124748758-124749046 | Common:3; Rare:64 | ||||
chr5:126595167-126595324 | Common:2; Rare:74; Clinvar:5; Clinvar (benign):7 | ||||
chr5:126776902-126777175 | Common:1; Rare:109; Clinvar:4; Clinvar (benign):3 | ||||
chr5:127290654-127290876 | Rare:45 | ||||
chr5:129460114-129460323 | Common:4; Rare:33 | ||||
chr5:131170670-131170993 | Common:1; Rare:73; Clinvar (benign):1 | ||||
chr5:131635160-131635446 | Common:1; Rare:109 |