Variant report

Variant	rs2287325
Chromosome Location	chr2:40803821-40803822
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10172760	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10183378	0.85[EUR][1000 genomes]
rs10183583	0.85[EUR][1000 genomes]
rs11124748	0.93[EUR][1000 genomes]
rs11124749	0.93[EUR][1000 genomes]
rs12993030	0.88[EUR][1000 genomes]
rs2042017	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2193560	0.85[EUR][1000 genomes]
rs2193561	0.83[EUR][1000 genomes]
rs2193562	0.85[EUR][1000 genomes]
rs2287324	0.85[EUR][1000 genomes]
rs42800	0.81[CEU][hapmap];0.89[TSI][hapmap]
rs42816	0.81[EUR][1000 genomes]
rs733297	0.92[EUR][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	nsv529606	chr2:40206280-40896881	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv873911	chr2:40423454-41161464	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv873917	chr2:40710953-41015998	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1000872	chr2:40791221-40829099	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40801200-40804200	Weak transcription	NHDF-Ad	bronchial
2	chr2:40803600-40804000	Weak transcription	NHLF	lung

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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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