Variant report

Variant	rs543934209
Chromosome Location	chr9:8281865-8281866
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8414	chr9:7827373-8511613	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1016723	chr9:8223541-8303017	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
3	nsv1031472	chr9:8250901-8712547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv892223	chr9:8258921-8318948	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS	miRNA target site	n/a	inside rSNPs	diseases
5	nsv892224	chr9:8263737-8338431	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS	miRNA target site	n/a	inside rSNPs	diseases
6	esv2761490	chr9:8278669-8283494	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3481878	chr9:8280765-8286383	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3481879	chr9:8280808-8286337	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3481880	chr9:8280808-8286337	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv2755828	chr9:8280950-8284789	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3693016	chr9:8280950-8284965	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8276000-8284600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:8281200-8282400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr9:8281400-8282400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:8281600-8282000	Enhancers	Fetal Intestine Small	intestine
5	chr9:8281600-8282000	Enhancers	Dnd41	blood
6	chr9:8281800-8282200	Enhancers	Fetal Intestine Large	intestine

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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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