Variant report

Variant	rs116627210
Chromosome Location	chr3:34120332-34120333
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv522881	chr3:33736126-34241686	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	esv3525372	chr3:34118598-34121396	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	n/a
3	esv3525376	chr3:34118998-34121296	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
4	esv3464237	chr3:34119596-34120451	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
5	esv3525371	chr3:34119622-34120420	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
6	esv3525374	chr3:34119629-34120440	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	inside rSNPs	n/a
7	esv3525375	chr3:34119686-34120377	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	n/a
8	esv19091	chr3:34119735-34120333	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	inside rSNPs	n/a
9	esv3464238	chr3:34119743-34120333	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
10	esv3525377	chr3:34119743-34120333	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34115800-34120400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr3:34119000-34120600	Enhancers	Fetal Brain Male	brain
3	chr3:34119200-34120400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr3:34119400-34120400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:34119600-34120600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr3:34119800-34120400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr3:34119800-34120600	Enhancers	GM12878-XiMat	blood
8	chr3:34120000-34120400	Enhancers	Brain Germinal Matrix	brain
9	chr3:34120200-34120800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:34120200-34121200	Enhancers	Primary hematopoietic stem cells short term culture	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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