Variant report

Variant	rs6839192
Chromosome Location	chr4:90999769-90999770
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1031123	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1031125	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11929774	0.83[EUR][1000 genomes]
rs11931255	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12648916	0.81[EUR][1000 genomes]
rs13104173	0.83[EUR][1000 genomes]
rs13117400	0.83[EUR][1000 genomes]
rs13122257	0.82[EUR][1000 genomes]
rs13122493	0.93[AFR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13127674	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1443797	0.83[EUR][1000 genomes]
rs1808952	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1975488	0.93[AFR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2197291	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35049792	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35474064	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3919723	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4626162	0.80[EUR][1000 genomes]
rs56300941	0.82[EUR][1000 genomes]
rs6532211	0.82[EUR][1000 genomes]
rs6812321	0.81[EUR][1000 genomes]
rs6813752	0.82[EUR][1000 genomes]
rs6815240	0.83[EUR][1000 genomes]
rs6816256	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6819864	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6826127	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6830566	0.81[EUR][1000 genomes]
rs6842029	0.82[EUR][1000 genomes]
rs722937	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs755053	0.81[EUR][1000 genomes]
rs7655785	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7662081	0.81[EUR][1000 genomes]
rs7670600	0.81[EUR][1000 genomes]
rs7671006	0.81[EUR][1000 genomes]
rs7671248	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7675130	0.82[EUR][1000 genomes]
rs7679917	0.80[ASN][1000 genomes]
rs7684512	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs894803	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv1012406	chr4:90167781-91166787	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv949454	chr4:90272120-91156917	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv470053	chr4:90879613-91439573	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv879537	chr4:90883047-91165346	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
5	nsv931074	chr4:90970476-91753697	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv830006	chr4:90971656-91186340	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
7	nsv879538	chr4:90993172-91080308	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:90990800-90999800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:90996000-91002800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:90996000-91002800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:90996200-90999800	Weak transcription	GM12878-XiMat	blood
5	chr4:90997200-90999800	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr4:90998600-91000400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:90998800-91000400	Enhancers	NHEK	skin
8	chr4:90998800-91003000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:90999000-90999800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:90999600-91000600	Enhancers	Monocytes-CD14+_RO01746	blood

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