Variant report

Variant	rs9591018
Chromosome Location	chr13:47840655-47840656
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10220095	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13378547	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1413075	0.93[EUR][1000 genomes]
rs17069824	0.93[ASN][1000 genomes]
rs2065563	0.95[EUR][1000 genomes]
rs7320763	0.93[EUR][1000 genomes]
rs7330865	0.93[EUR][1000 genomes]
rs8000212	0.93[EUR][1000 genomes]
rs8001433	0.91[EUR][1000 genomes]
rs9316272	0.90[EUR][1000 genomes]
rs9316273	0.90[ASN][1000 genomes]
rs9316290	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9534600	0.89[EUR][1000 genomes]
rs9591015	0.87[ASN][1000 genomes]
rs9591016	0.90[EUR][1000 genomes]
rs9591026	0.93[EUR][1000 genomes]
rs9591028	0.93[EUR][1000 genomes]
rs9591029	0.93[EUR][1000 genomes]
rs9595631	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9595632	1.00[ASN][1000 genomes]
rs9595633	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9595636	0.93[ASN][1000 genomes]
rs9595637	0.81[ASN][1000 genomes]
rs9595638	0.93[ASN][1000 genomes]
rs9595643	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763019	chr13:47348229-48123447	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv3394678	chr13:47678184-48039379	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv832599	chr13:47703075-47873855	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv455878	chr13:47822976-47842680	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	lncRNA	n/a	inside rSNPs	diseases
5	nsv561586	chr13:47822976-47842680	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	lncRNA	n/a	inside rSNPs	diseases
6	nsv1046560	chr13:47826023-47854425	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv527824	chr13:47839420-47841000	Inactive region	lncRNA	n/a	inside rSNPs	diseases

No data

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

No data

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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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