Variant report

Variant	rs4956394
Chromosome Location	chr4:142430894-142430895
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs4956296	0.85[AMR][1000 genomes]
rs4956379	0.85[AMR][1000 genomes]
rs4956383	0.85[AMR][1000 genomes]
rs57502347	0.85[AMR][1000 genomes]
rs58286582	0.85[AFR][1000 genomes]
rs60272797	0.85[AMR][1000 genomes]
rs72940626	0.85[AMR][1000 genomes]
rs72940633	0.85[AMR][1000 genomes]
rs72940637	0.85[AMR][1000 genomes]
rs72940639	0.85[AMR][1000 genomes]
rs72940653	0.85[AMR][1000 genomes]
rs72940673	0.85[AMR][1000 genomes]
rs72940682	0.85[AMR][1000 genomes]
rs72942598	0.85[AMR][1000 genomes]
rs72942601	0.85[AMR][1000 genomes]
rs7691233	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7692579	0.85[AMR][1000 genomes]
rs7693947	0.85[AMR][1000 genomes]

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	nsv880172	chr4:142355535-142565089	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv880173	chr4:142355535-142666106	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830094	chr4:142411738-142567788	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv964260	chr4:142413497-142434363	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv967689	chr4:142421303-142433549	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142430400-142431400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell

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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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