Variant report

Variant	rs6591855
Chromosome Location	chr11:64265750-64265751
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11231799	1.00[ASN][1000 genomes]
rs11231811	0.82[ASN][1000 genomes]
rs11231812	0.82[ASN][1000 genomes]
rs1207462	1.00[EUR][1000 genomes]
rs12285139	0.86[ASN][1000 genomes]
rs12289479	0.86[ASN][1000 genomes]
rs12575515	1.00[EUR][1000 genomes]
rs17159251	1.00[EUR][1000 genomes]
rs34318219	1.00[EUR][1000 genomes]
rs490720	1.00[EUR][1000 genomes]
rs539008	1.00[EUR][1000 genomes]
rs554812	1.00[EUR][1000 genomes]
rs56810477	0.82[ASN][1000 genomes]
rs569741	1.00[EUR][1000 genomes]
rs575081	1.00[EUR][1000 genomes]
rs58010797	1.00[EUR][1000 genomes]
rs58488481	1.00[EUR][1000 genomes]
rs6421689	0.84[YRI][hapmap]
rs7112596	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs7115265	1.00[EUR][1000 genomes]
rs7119291	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs7124976	1.00[EUR][1000 genomes]
rs7127435	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs71579879	1.00[EUR][1000 genomes]
rs72559736	1.00[EUR][1000 genomes]
rs73488285	1.00[EUR][1000 genomes]
rs73488288	1.00[EUR][1000 genomes]
rs73488293	1.00[EUR][1000 genomes]
rs73488297	1.00[EUR][1000 genomes]
rs73490206	1.00[EUR][1000 genomes]
rs73490261	1.00[EUR][1000 genomes]
rs7947416	1.00[EUR][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	nsv832187	chr11:64121969-64312300	Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv1035485	chr11:64228847-64354869	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64265000-64268000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr11:64265400-64266800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr11:64265400-64267200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:64265400-64269200	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr11:64265600-64266400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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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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