Variant report

Variant	rs10437677
Chromosome Location	chr11:108865815-108865816
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10789701	0.91[EUR][1000 genomes]
rs11600003	0.84[ASN][1000 genomes]
rs1425796	0.81[ASN][1000 genomes]
rs4753855	0.84[ASN][1000 genomes]
rs57748924	0.85[ASN][1000 genomes]
rs61912833	0.84[ASN][1000 genomes]
rs7113437	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][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	nsv898389	chr11:108724639-108891986	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv1040650	chr11:108859584-109174553	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription	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	chr11:108865000-108866600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr11:108865200-108866000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr11:108865400-108866400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:108865600-108866000	Active TSS	Monocytes-CD14+_RO01746	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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