Variant report

Variant	rs35830942
Chromosome Location	chr6:25233911-25233912
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11755567	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11760097	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11964920	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11969842	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13201672	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2064207	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2064208	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34044829	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34816485	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35133360	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35528016	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35618329	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35997400	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs58597163	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59060048	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59525347	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9461124	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9467445	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9467446	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023989	chr6:24930362-25285679	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	nsv1025694	chr6:25136860-25309450	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv1020774	chr6:25154152-25285679	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv538161	chr6:25154152-25285679	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv462663	chr6:25156197-25234884	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv601167	chr6:25156197-25234884	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv883483	chr6:25200842-25272435	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr6:25231000-25239000	Weak transcription	Osteobl	bone
2	chr6:25231200-25234200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr6:25232400-25234200	Enhancers	Fetal Brain Male	brain
4	chr6:25232800-25234000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:25233000-25234000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:25233000-25234000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:25233000-25234000	Enhancers	NHLF	lung
8	chr6:25233600-25234000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:25233600-25234000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:25233600-25234000	Enhancers	Fetal Stomach	stomach
11	chr6:25233800-25234000	Enhancers	NHDF-Ad	bronchial

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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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