Variant report

Variant	rs59300876
Chromosome Location	chr11:59182131-59182132
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs17153691	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs17153714	0.86[EUR][1000 genomes]
rs17153751	0.82[EUR][1000 genomes]
rs1955199	0.86[EUR][1000 genomes]
rs1955200	0.86[EUR][1000 genomes]
rs57417127	0.81[ASN][1000 genomes]
rs57556536	1.00[AFR][1000 genomes]
rs58090903	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59966846	1.00[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs61001950	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs61381338	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72472134	1.00[AFR][1000 genomes]
rs72472135	1.00[AFR][1000 genomes]
rs72472136	0.81[ASN][1000 genomes]
rs72472137	1.00[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs72472138	1.00[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7929185	0.81[ASN][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	nsv1050013	chr11:58394598-59221090	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1046084	chr11:59034871-59314519	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv541052	chr11:59119390-59185103	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1047952	chr11:59124719-59221606	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59181400-59182400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr11:59181600-59184200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr11:59181800-59182400	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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