Variant report

Variant	rs11630774
Chromosome Location	chr15:54562362-54562363
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10518761	0.91[CEU][hapmap]
rs11629837	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs11630328	0.89[EUR][1000 genomes]
rs11630329	0.90[EUR][1000 genomes]
rs11635750	0.88[EUR][1000 genomes]
rs11636703	0.91[CEU][hapmap];0.91[EUR][1000 genomes]
rs11637720	0.81[CEU][hapmap];0.89[EUR][1000 genomes]
rs11638873	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs12101497	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs12437533	0.87[CHB][hapmap]
rs12441610	0.81[CHB][hapmap]
rs16953182	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs16974384	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs16974387	0.90[CEU][hapmap];0.88[EUR][1000 genomes]
rs16974390	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs16974409	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs16974410	0.81[CHB][hapmap]
rs16974431	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs16974443	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs16974464	0.91[CEU][hapmap]
rs2414293	0.88[EUR][1000 genomes]
rs4502150	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs4776221	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs4776223	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs62010056	0.88[EUR][1000 genomes]
rs62011962	0.93[EUR][1000 genomes]
rs6493671	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs8028896	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs8033976	0.81[CHB][hapmap]
rs8039159	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs9806492	0.81[CEU][hapmap]

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	nsv1052235	chr15:53677524-54618723	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542388	chr15:53677524-54618723	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	esv1845471	chr15:54556063-54685463	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr15:54547000-54652600	Weak transcription	Fetal Lung	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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