Variant report

Variant	rs16847786
Chromosome Location	chr2:213012030-213012031
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs16847714	0.82[YRI][hapmap]
rs16847732	0.82[YRI][hapmap]
rs16847752	0.82[YRI][hapmap]
rs16847762	0.82[YRI][hapmap];0.81[AFR][1000 genomes]
rs16847767	0.82[YRI][hapmap]
rs16847769	0.82[YRI][hapmap]
rs16847773	0.82[YRI][hapmap]
rs16847776	0.82[YRI][hapmap];0.81[AFR][1000 genomes]
rs16847781	0.85[YRI][hapmap];0.83[AFR][1000 genomes]
rs16847782	0.83[AFR][1000 genomes]
rs16847802	1.00[YRI][hapmap]
rs16847805	1.00[YRI][hapmap]
rs55760492	0.94[AFR][1000 genomes]
rs58176578	0.92[AFR][1000 genomes]
rs59383771	0.81[AFR][1000 genomes]
rs59942033	0.85[AFR][1000 genomes]
rs73987242	0.81[AFR][1000 genomes]
rs73987243	0.81[AFR][1000 genomes]
rs73987244	0.83[AFR][1000 genomes]
rs73987245	0.81[AFR][1000 genomes]
rs73987246	0.81[AFR][1000 genomes]
rs73987247	0.81[AFR][1000 genomes]
rs73987248	0.83[AFR][1000 genomes]
rs73987249	0.83[AFR][1000 genomes]
rs73987250	0.81[AFR][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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213010800-213012600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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