Variant report

Variant	rs536802683
Chromosome Location	chr11:56946813-56946814
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915640	chr11:56814841-57139786	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv482317	chr11:56857026-57028631	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv12593	chr11:56946787-56948827	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56946200-56947800	Enhancers	Fetal Brain Male	brain
2	chr11:56946400-56947400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr11:56946600-56947000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
4	chr11:56946600-56947200	Flanking Active TSS	Fetal Brain Female	brain
5	chr11:56946600-56948600	Enhancers	Pancreas	Pancrea
6	chr11:56946800-56947000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
7	chr11:56946800-56947200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr11:56946800-56947200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
9	chr11:56946800-56947200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr11:56946800-56947200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
11	chr11:56946800-56948600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell

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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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