Variant report

Variant	rs11787493
Chromosome Location	chr8:10455438-10455439
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10108562	1.00[ASN][1000 genomes]
rs11774008	1.00[ASN][1000 genomes]
rs11775794	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11776423	1.00[ASN][1000 genomes]
rs11776454	1.00[ASN][1000 genomes]
rs11777184	1.00[ASN][1000 genomes]
rs11778788	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11778815	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11779652	1.00[ASN][1000 genomes]
rs11780167	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11780436	0.81[CEU][hapmap]
rs11780868	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11781718	1.00[ASN][1000 genomes]
rs11783848	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11785876	1.00[ASN][1000 genomes]
rs11786322	0.82[EUR][1000 genomes]
rs11786688	1.00[ASN][1000 genomes]
rs11787384	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11992557	0.82[EUR][1000 genomes]
rs13249905	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13259038	1.00[CHB][hapmap]
rs13269403	1.00[CHB][hapmap]
rs28361533	1.00[ASN][1000 genomes]
rs28577240	1.00[ASN][1000 genomes]
rs34994999	1.00[ASN][1000 genomes]
rs4320513	1.00[ASN][1000 genomes]
rs4591993	1.00[ASN][1000 genomes]
rs4840494	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4840495	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4840496	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4841364	0.81[CEU][hapmap]
rs4841367	0.81[CEU][hapmap];1.00[ASN][1000 genomes]
rs4841379	1.00[ASN][1000 genomes]
rs4841390	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4841391	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4841394	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4841395	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4841396	1.00[AMR][1000 genomes]
rs4841397	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4841400	1.00[ASN][1000 genomes]
rs4841406	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs56096665	1.00[ASN][1000 genomes]
rs58842562	1.00[ASN][1000 genomes]
rs60930396	1.00[ASN][1000 genomes]
rs61743179	1.00[ASN][1000 genomes]
rs6601486	1.00[ASN][1000 genomes]
rs6981847	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs73662849	1.00[ASN][1000 genomes]
rs73662851	1.00[ASN][1000 genomes]
rs73662852	1.00[ASN][1000 genomes]
rs73662853	1.00[ASN][1000 genomes]
rs73662854	1.00[ASN][1000 genomes]
rs73662855	1.00[ASN][1000 genomes]
rs73662857	1.00[ASN][1000 genomes]
rs73662858	1.00[ASN][1000 genomes]
rs7846306	1.00[CHB][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030934	chr8:10065169-10561161	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1025557	chr8:10216726-10555187	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
6	nsv610267	chr8:10268736-10526742	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv610268	chr8:10331636-10486652	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
8	nsv1025251	chr8:10343591-10488557	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv1015932	chr8:10357101-10597856	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
10	nsv610269	chr8:10416017-10461484	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv610271	chr8:10438796-10459203	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv890351	chr8:10439902-10482372	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
13	nsv1031279	chr8:10448142-10501380	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
14	nsv1022682	chr8:10453091-10501380	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10448200-10456200	Weak transcription	Liver	Liver
2	chr8:10451800-10490000	Weak transcription	Right Atrium	heart
3	chr8:10452000-10455800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:10452000-10455800	Weak transcription	NH-A	brain
5	chr8:10453600-10455600	Weak transcription	HSMM	muscle
6	chr8:10453600-10455800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr8:10453800-10457600	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr8:10454400-10457400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr8:10454600-10455600	Enhancers	Spleen	Spleen
10	chr8:10455200-10455600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
11	chr8:10455200-10455800	Enhancers	NHEK	skin
12	chr8:10455200-10456400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:10455200-10456800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr8:10455200-10457000	Enhancers	Esophagus	oesophagus
15	chr8:10455200-10457200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr8:10455200-10457400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:10455200-10457400	Enhancers	Ovary	ovary
18	chr8:10455400-10455800	Enhancers	Hela-S3	cervix
19	chr8:10455400-10456200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:10455400-10456400	Enhancers	Placenta Amnion	Placenta Amnion
21	chr8:10455400-10457000	Enhancers	HMEC	breast

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