Variant report

Variant	rs144312798
Chromosome Location	chr11:84878263-84878264
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv527535	chr11:84724795-84895033	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv528491	chr11:84724795-84895033	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
4	nsv1052380	chr11:84864551-84920320	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv898042	chr11:84877221-84965437	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84866000-84881200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr11:84866400-84878400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr11:84866400-84878400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr11:84877400-84878400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr11:84878200-84878800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr11:84878200-84879000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr11:84878200-84879000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:84878200-84879200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr11:84878200-84879200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr11:84878200-84879200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr11:84878200-84879400	Enhancers	NHEK	skin

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

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