Variant report

Variant	rs11675414
Chromosome Location	chr2:11191221-11191222
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10164900	0.80[EUR][1000 genomes]
rs10174308	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10185403	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10205830	0.80[EUR][1000 genomes]
rs10221871	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10439232	0.83[EUR][1000 genomes]
rs12994083	0.82[EUR][1000 genomes]
rs13016104	0.85[EUR][1000 genomes]
rs13032732	0.85[EUR][1000 genomes]
rs34481886	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs71439044	0.83[AMR][1000 genomes];0.82[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	nsv833392	chr2:11054580-11235239	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv580971	chr2:11175395-11226507	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11191000-11191400	Enhancers	Fetal Brain Male	brain
2	chr2:11191000-11196800	Weak transcription	Fetal Brain Female	brain

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

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