Variant report

Variant	rs191235812
Chromosome Location	chr3:23390630-23390631
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014701	chr3:23257658-23416094	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv589947	chr3:23277838-23403943	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1002823	chr3:23277838-23623083	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1007373	chr3:23367952-23710331	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv876624	chr3:23385877-23483536	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv876625	chr3:23390301-23509597	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23367400-23391400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr3:23368000-23391000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:23384400-23391800	Weak transcription	Primary B cells from cord blood	blood
4	chr3:23386600-23403800	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr3:23389400-23391000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr3:23390000-23390800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
7	chr3:23390200-23391200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
8	chr3:23390400-23390800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
9	chr3:23390400-23391000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr3:23390400-23391200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr3:23390400-23391200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr3:23390600-23391200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr3:23390600-23391200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr3:23390600-23391200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
15	chr3:23390600-23391200	Enhancers	Primary B cells from peripheral blood	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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