Variant report

Variant	rs10037935
Chromosome Location	chr5:79632924-79632925
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10060692	1.00[CEU][hapmap];0.91[CHB][hapmap]
rs10064457	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs11749321	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12055120	0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs12523297	1.00[CEU][hapmap]
rs13179066	0.90[JPT][hapmap]
rs16876315	0.92[CEU][hapmap];0.95[CHB][hapmap]
rs1990858	0.81[ASN][1000 genomes]
rs4133093	0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs4704663	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7703252	0.83[JPT][hapmap]
rs879738	0.90[JPT][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	nsv948807	chr5:79549207-79805765	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv518480	chr5:79586085-79748382	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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