Variant report

Variant	rs66499837
Chromosome Location	chr18:12195550-12195551
allele	A/G
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:24)

rs_ID	r²[population]
rs11874561	0.84[ASN][1000 genomes]
rs11875015	0.81[ASN][1000 genomes]
rs11875591	0.84[ASN][1000 genomes]
rs11876891	0.81[ASN][1000 genomes]
rs12959671	0.82[ASN][1000 genomes]
rs12960683	0.84[ASN][1000 genomes]
rs12963390	0.84[ASN][1000 genomes]
rs13381106	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17594826	0.84[ASN][1000 genomes]
rs34045099	0.84[ASN][1000 genomes]
rs34652396	0.84[ASN][1000 genomes]
rs34774742	0.81[ASN][1000 genomes]
rs35626710	0.81[ASN][1000 genomes]
rs35640729	0.84[ASN][1000 genomes]
rs4797621	0.84[ASN][1000 genomes]
rs4797641	0.81[ASN][1000 genomes]
rs57698452	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58779678	0.84[ASN][1000 genomes]
rs71351456	0.92[ASN][1000 genomes]
rs72879124	0.81[ASN][1000 genomes]
rs72880946	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8084767	0.84[ASN][1000 genomes]
rs8086282	0.84[ASN][1000 genomes]
rs8093087	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063125	chr18:12046892-12918251	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
2	nsv1055343	chr18:12107012-12226356	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv491873	chr18:12159445-12739784	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
4	nsv960252	chr18:12161216-12220798	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	4 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	chr18:12195400-12196000	Enhancers	HUVEC	blood vessel

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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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