Variant report

Variant	rs11126105
Chromosome Location	chr2:67187510-67187511
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11126104	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12620024	0.87[ASN][1000 genomes]
rs1420366	0.86[CEU][hapmap]
rs17032776	0.97[EUR][1000 genomes]
rs17032792	0.87[ASN][1000 genomes]
rs17032810	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[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	nsv1008584	chr2:67168244-67703601	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535775	chr2:67168244-67703601	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67184200-67190000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr2:67184800-67189800	Weak transcription	Fetal Lung	lung
3	chr2:67185400-67188800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr2:67185400-67193400	Weak transcription	Pancreas	Pancrea
5	chr2:67186400-67187600	Enhancers	Colon Smooth Muscle	Colon
6	chr2:67186600-67187600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr2:67187200-67187600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:67187200-67187800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr2:67187400-67187600	Enhancers	Spleen	Spleen
10	chr2:67187400-67187800	Enhancers	Fetal Heart	heart
11	chr2:67187400-67188000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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