Variant report

Variant	rs1276270
Chromosome Location	chr11:102549484-102549485
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11821641	1.00[ASN][1000 genomes]
rs11828553	1.00[ASN][1000 genomes]
rs12272186	1.00[ASN][1000 genomes]
rs12289076	1.00[ASN][1000 genomes]
rs1276266	0.95[AFR][1000 genomes]
rs1276267	0.80[AMR][1000 genomes]
rs1276269	0.96[YRI][hapmap];0.94[AFR][1000 genomes]
rs1276271	0.80[AMR][1000 genomes]
rs12785370	1.00[ASN][1000 genomes]
rs12794384	1.00[ASN][1000 genomes]
rs12802760	1.00[ASN][1000 genomes]
rs12803000	1.00[ASN][1000 genomes]
rs1291325	0.80[AMR][1000 genomes]
rs1296221	0.89[AFR][1000 genomes]
rs17099394	1.00[ASN][1000 genomes]
rs17099425	1.00[ASN][1000 genomes]
rs17099427	1.00[ASN][1000 genomes]
rs17099450	1.00[ASN][1000 genomes]
rs1940472	0.80[AMR][1000 genomes]
rs2846343	0.80[AMR][1000 genomes]
rs2846368	0.80[AMR][1000 genomes]
rs28478243	1.00[ASN][1000 genomes]
rs28662184	1.00[ASN][1000 genomes]
rs33927742	1.00[ASN][1000 genomes]
rs33982701	1.00[ASN][1000 genomes]
rs34347515	1.00[ASN][1000 genomes]
rs34472552	1.00[ASN][1000 genomes]
rs34802753	1.00[ASN][1000 genomes]
rs35248432	1.00[ASN][1000 genomes]
rs35594127	1.00[ASN][1000 genomes]
rs35602886	1.00[ASN][1000 genomes]
rs35866072	1.00[ASN][1000 genomes]
rs57646005	1.00[ASN][1000 genomes]
rs73588675	1.00[ASN][1000 genomes]
rs9704711	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832252	chr11:102445479-102627879	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1037454	chr11:102487521-102601233	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv541156	chr11:102487521-102601233	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102548000-102549600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:102548600-102556000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr11:102549000-102554400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr11:102549400-102551400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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