Variant report

Variant	rs11774085
Chromosome Location	chr8:96020877-96020878
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 101 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10086541	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10092003	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10093594	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10096455	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10097930	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10098197	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10098453	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10100089	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10103841	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10105437	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10106491	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10110635	0.93[EUR][1000 genomes]
rs10111154	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10111300	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10112230	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10113545	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1031388	0.93[ASN][1000 genomes]
rs10504939	0.81[AFR][1000 genomes]
rs11776186	0.81[AFR][1000 genomes]
rs11776189	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11778553	0.81[AFR][1000 genomes]
rs11779506	0.87[ASN][1000 genomes]
rs11779698	0.81[AFR][1000 genomes]
rs11780130	0.81[AFR][1000 genomes]
rs11780931	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11781001	0.93[ASN][1000 genomes]
rs11781040	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11781397	0.81[AFR][1000 genomes]
rs11781619	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11781757	0.81[AFR][1000 genomes]
rs11782590	0.81[AFR][1000 genomes]
rs11782818	0.81[AFR][1000 genomes]
rs11783262	0.81[AFR][1000 genomes]
rs11783878	0.81[AFR][1000 genomes]
rs11783985	0.81[AFR][1000 genomes]
rs11784178	0.90[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11784212	0.81[AFR][1000 genomes]
rs11786380	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11786878	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11787303	0.81[AFR][1000 genomes]
rs13279040	0.81[ASN][1000 genomes]
rs1545480	0.87[ASN][1000 genomes]
rs16917224	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16917233	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17665714	0.81[AFR][1000 genomes]
rs17665737	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2340536	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2599711	0.87[ASN][1000 genomes]
rs2599713	0.93[ASN][1000 genomes]
rs2599714	0.93[ASN][1000 genomes]
rs2599715	0.93[ASN][1000 genomes]
rs2678823	0.93[ASN][1000 genomes]
rs2678829	1.00[ASN][1000 genomes]
rs28363725	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28378156	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28406132	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28419772	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28440026	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28477467	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28496357	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28616734	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28651964	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28712702	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34700722	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35518242	0.81[ASN][1000 genomes]
rs4323442	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56901035	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57890591	0.81[AFR][1000 genomes]
rs57925408	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58282276	0.81[AFR][1000 genomes]
rs58314911	0.81[AFR][1000 genomes]
rs60003497	0.81[AFR][1000 genomes]
rs61591488	0.81[AFR][1000 genomes]
rs61596977	0.82[EUR][1000 genomes]
rs6471505	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6471506	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6651271	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6651272	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6985880	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6989862	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7002940	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7008542	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71532343	0.81[ASN][1000 genomes]
rs73276406	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73276417	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73276437	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73276439	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73276444	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7812312	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7818688	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7826046	0.90[ASN][1000 genomes]
rs7826196	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7832570	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7842703	0.90[ASN][1000 genomes]
rs7842715	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9297950	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9297951	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv508520	chr8:95939373-96140068	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv524876	chr8:96000919-96027306	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11774085	INTS8	Cis_1M	lymphoblastoid	RTeQTL
rs11774085	C8orf38	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95977400-96024200	Weak transcription	Aorta	Aorta
2	chr8:96001200-96023400	Weak transcription	Liver	Liver
3	chr8:96003200-96032600	Weak transcription	Gastric	stomach
4	chr8:96009000-96036400	Weak transcription	Spleen	Spleen
5	chr8:96009800-96023000	Weak transcription	Adipose Nuclei	Adipose
6	chr8:96014600-96021600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:96015600-96021600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:96016000-96021600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr8:96016200-96021600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr8:96016400-96021400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr8:96016400-96021600	Weak transcription	Brain Germinal Matrix	brain
12	chr8:96018400-96023000	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr8:96018800-96021600	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr8:96019800-96023200	Weak transcription	Lung	lung
15	chr8:96020200-96022600	Weak transcription	A549	lung
16	chr8:96020400-96021600	Weak transcription	HepG2	liver
17	chr8:96020600-96022000	Enhancers	Fetal Stomach	stomach
18	chr8:96020800-96021000	Enhancers	Fetal Muscle Trunk	muscle

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