Variant report

Variant	rs192927
Chromosome Location	chr2:211900425-211900426
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10804187	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1087945	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1087949	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1088222	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11683805	0.94[ASN][1000 genomes]
rs11692975	0.93[ASN][1000 genomes]
rs12623879	0.96[ASN][1000 genomes]
rs13015456	0.96[ASN][1000 genomes]
rs35455807	0.88[ASN][1000 genomes]
rs35501999	0.87[ASN][1000 genomes]
rs418123	0.93[ASN][1000 genomes]
rs56371952	0.98[ASN][1000 genomes]
rs796230	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

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	nsv1012193	chr2:211684524-212072213	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv875772	chr2:211893388-211946057	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211900200-211900800	Enhancers	Brain Angular Gyrus	brain
2	chr2:211900400-211900600	Enhancers	Brain Germinal Matrix	brain
3	chr2:211900400-211900600	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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