Variant report

Variant	rs10110635
Chromosome Location	chr8:96025069-96025070
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:95979420..95981585-chr8:96022909..96025497,2	MCF-7	breast:
2	chr8:96022721..96025517-chr8:96026848..96029515,2	MCF-7	breast:

Extended variants
information (count: 68 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10086541	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10092003	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10093594	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10096455	0.95[EUR][1000 genomes]
rs10097930	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10098197	0.97[EUR][1000 genomes]
rs10098453	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10100089	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10103841	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10105437	0.97[EUR][1000 genomes]
rs10106491	0.97[EUR][1000 genomes]
rs10111154	0.94[EUR][1000 genomes]
rs10111300	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10112230	0.97[EUR][1000 genomes]
rs10113545	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11774085	0.93[EUR][1000 genomes]
rs11776189	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11780931	0.97[EUR][1000 genomes]
rs11781001	0.86[EUR][1000 genomes]
rs11781040	0.96[EUR][1000 genomes]
rs11781619	0.91[EUR][1000 genomes]
rs11784178	0.90[EUR][1000 genomes]
rs11786380	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11786878	0.99[EUR][1000 genomes]
rs16917224	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16917233	0.97[EUR][1000 genomes]
rs2340536	0.91[EUR][1000 genomes]
rs28363725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28378156	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28406132	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28419772	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28440026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28477467	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs28496357	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs28616734	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28651964	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28712702	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34700722	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4323442	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56901035	0.97[EUR][1000 genomes]
rs57925408	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61596977	0.87[EUR][1000 genomes]
rs6471505	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6471506	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6651271	0.97[EUR][1000 genomes]
rs6651272	0.97[EUR][1000 genomes]
rs6985880	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6989862	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7002940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7008542	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73276406	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73276417	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73276437	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73276439	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73276444	0.97[EUR][1000 genomes]
rs7812312	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7818688	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7826046	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs7826196	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7832570	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7842703	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7842715	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9297950	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9297951	0.97[EUR][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
rs10110635	INTS8	Cis_1M	lymphoblastoid	RTeQTL
rs10110635	C8orf38	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96003200-96032600	Weak transcription	Gastric	stomach
2	chr8:96009000-96036400	Weak transcription	Spleen	Spleen
3	chr8:96021600-96027000	Enhancers	HepG2	liver
4	chr8:96021800-96025400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:96023000-96025600	Enhancers	Osteobl	bone
6	chr8:96023200-96030200	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr8:96023400-96025200	Enhancers	Liver	Liver
8	chr8:96023400-96026000	Weak transcription	Left Ventricle	heart
9	chr8:96023400-96029000	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr8:96023400-96032600	Weak transcription	Right Atrium	heart
11	chr8:96023400-96036600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:96023600-96025400	Enhancers	NHDF-Ad	bronchial
13	chr8:96024800-96026000	Weak transcription	A549	lung
14	chr8:96024800-96026200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr8:96024800-96026400	Weak transcription	NHLF	lung
16	chr8:96024800-96036400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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