Variant report

Variant	rs6732730
Chromosome Location	chr2:213009392-213009393
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11903314	0.82[YRI][hapmap];0.91[AMR][1000 genomes]
rs16847741	0.82[AMR][1000 genomes]
rs16847746	0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs16847747	0.82[AMR][1000 genomes]
rs16847775	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16847783	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58725196	0.94[AFR][1000 genomes]
rs58834228	0.82[AMR][1000 genomes]
rs60076681	0.82[AMR][1000 genomes]
rs6723461	1.00[YRI][hapmap];0.81[AMR][1000 genomes]
rs6746409	1.00[CEU][hapmap]
rs7559605	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7560757	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7573642	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7589512	1.00[CEU][hapmap]
rs7608211	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011572	chr2:212840066-213152279	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv875805	chr2:212891401-213164837	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv875806	chr2:212997024-213211067	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213001400-213009400	Weak transcription	Fetal Heart	heart
2	chr2:213003400-213009400	Weak transcription	Fetal Intestine Small	intestine
3	chr2:213009000-213009400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:213009200-213011000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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