Variant report

Variant	rs4643905
Chromosome Location	chr5:59621090-59621091
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10514891	0.95[LWK][hapmap];0.89[YRI][hapmap];0.80[AFR][1000 genomes]
rs12109374	1.00[YRI][hapmap]
rs16877877	1.00[MEX][hapmap]
rs4640751	1.00[ASW][hapmap];0.83[MKK][hapmap];0.90[YRI][hapmap];1.00[AMR][1000 genomes]
rs58718949	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60264107	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6869344	1.00[MEX][hapmap]
rs6874388	0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6879098	0.86[YRI][hapmap];1.00[AMR][1000 genomes]
rs6879388	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73104773	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106737	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106738	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106748	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106750	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7341019	0.92[AMR][1000 genomes]
rs7703345	1.00[YRI][hapmap]
rs7721376	0.90[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025856	chr5:59188419-59928852	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv830316	chr5:59480269-59689829	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59619000-59623400	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59619200-59621200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr5:59619600-59621200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:59620000-59623600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:59620000-59625000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr5:59620400-59629400	Weak transcription	Aorta	Aorta
7	chr5:59620400-59631000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:59620600-59621400	Enhancers	iPS-18 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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