Variant report

Variant	rs9643371
Chromosome Location	chr8:61614884-61614885
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:61590866..61593326-chr8:61611712..61615687,3	MCF-7	breast:
2	chr8:61563289..61565598-chr8:61614731..61616834,3	MCF-7	breast:
3	chr8:61612592..61618600-chr8:61619190..61622495,7	MCF-7	breast:
4	chr8:61612691..61616083-chr8:61619050..61621954,3	K562	blood:
5	chr8:61590260..61597729-chr8:61611560..61624694,18	MCF-7	breast:
6	chr8:61614401..61615964-chr8:61617449..61618958,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000171316	Chromatin interaction

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10093135	0.84[ASN][1000 genomes]
rs1038352	0.81[ASN][1000 genomes]
rs10808711	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10808712	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10808713	0.89[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10957154	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10957155	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10957156	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10957158	0.81[ASN][1000 genomes]
rs11985638	0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11990117	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11990495	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11991467	0.81[ASN][1000 genomes]
rs11992809	0.89[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11993480	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11995234	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11997122	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12544305	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12681737	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13255519	0.89[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs13264014	0.84[ASN][1000 genomes]
rs13277976	0.81[ASN][1000 genomes]
rs1384688	0.80[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs1483206	0.84[ASN][1000 genomes]
rs16926407	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1905305	0.84[ASN][1000 genomes]
rs2035456	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2035457	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2054666	0.81[ASN][1000 genomes]
rs2054667	0.81[ASN][1000 genomes]
rs2128713	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2326598	0.81[ASN][1000 genomes]
rs2875984	0.81[ASN][1000 genomes]
rs4307377	0.89[CHB][hapmap]
rs4449834	0.90[CHB][hapmap]
rs4472560	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4500113	0.81[ASN][1000 genomes]
rs4526395	1.00[CHB][hapmap]
rs4737563	0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4737565	0.81[CEU][hapmap];0.90[CHB][hapmap]
rs4738815	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4738818	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4738821	0.81[ASN][1000 genomes]
rs4738822	0.81[ASN][1000 genomes]
rs4738824	0.81[ASN][1000 genomes]
rs4738831	0.90[CHB][hapmap]
rs4738832	0.90[CHB][hapmap]
rs6471894	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6471896	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6471897	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6471898	0.89[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6471901	0.81[ASN][1000 genomes]
rs6471903	0.84[CEU][hapmap];0.89[CHB][hapmap]
rs6471905	0.90[CHB][hapmap]
rs6988582	0.80[CEU][hapmap];0.80[EUR][1000 genomes]
rs6994180	0.84[ASN][1000 genomes]
rs6995557	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7000766	0.89[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7002806	0.81[ASN][1000 genomes]
rs7005873	0.89[CHB][hapmap]
rs7009754	0.81[ASN][1000 genomes]
rs7011972	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7012450	0.84[ASN][1000 genomes]
rs7017676	0.81[ASN][1000 genomes]
rs730085	0.89[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7814114	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7816126	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7816621	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7823484	0.81[ASN][1000 genomes]
rs7826035	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7834977	0.88[CHB][hapmap]
rs7836586	0.84[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7838426	0.84[ASN][1000 genomes]
rs7840098	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs7842389	0.80[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7842498	0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7843033	0.81[ASN][1000 genomes]
rs7845701	0.81[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7846065	0.84[ASN][1000 genomes]
rs900502	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9298040	0.84[ASN][1000 genomes]
rs9650201	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917756	chr8:60942299-61862796	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv831335	chr8:61497540-61688992	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv890945	chr8:61522008-61707725	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv824657	chr8:61555227-61626758	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
5	nsv1027929	chr8:61569620-61617812	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv1017564	chr8:61577791-61617812	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
7	nsv526196	chr8:61593569-61877623	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
8	nsv1019809	chr8:61597918-61624034	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv539631	chr8:61597918-61624034	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv6219	chr8:61599770-61644558	Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61594200-61617600	Weak transcription	Hela-S3	cervix
2	chr8:61597000-61619800	Weak transcription	HMEC	breast
3	chr8:61598200-61619800	Weak transcription	HepG2	liver
4	chr8:61603400-61616200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr8:61603400-61620600	Weak transcription	Fetal Intestine Large	intestine
6	chr8:61603400-61626200	Weak transcription	Fetal Thymus	thymus
7	chr8:61605800-61615400	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr8:61606400-61620400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr8:61607200-61619800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:61607400-61615400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:61607400-61619800	Weak transcription	Fetal Lung	lung
12	chr8:61607400-61627000	Weak transcription	Spleen	Spleen
13	chr8:61607600-61615000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr8:61607600-61615800	Weak transcription	Small Intestine	intestine
15	chr8:61607600-61616200	Weak transcription	Right Atrium	heart
16	chr8:61607600-61620400	Weak transcription	Fetal Muscle Leg	muscle
17	chr8:61607800-61615000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr8:61608200-61615000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr8:61608600-61615800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr8:61609200-61619800	Weak transcription	HSMM	muscle
21	chr8:61609200-61620400	Weak transcription	NH-A	brain
22	chr8:61610400-61615400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr8:61610600-61620000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr8:61610800-61615600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:61612400-61617400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr8:61612600-61616200	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr8:61612600-61616400	Enhancers	Fetal Heart	heart
28	chr8:61612600-61622000	Enhancers	Primary B cells from peripheral blood	blood
29	chr8:61612800-61616200	Enhancers	Primary B cells from cord blood	blood
30	chr8:61613000-61615200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr8:61613000-61615800	Enhancers	Fetal Brain Male	brain
32	chr8:61613200-61615000	Enhancers	Primary T cells from cord blood	blood
33	chr8:61613200-61616800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr8:61613400-61615400	Enhancers	K562	blood
35	chr8:61613400-61619800	Weak transcription	Gastric	stomach
36	chr8:61613600-61615000	Weak transcription	Brain Angular Gyrus	brain
37	chr8:61613600-61615000	Weak transcription	Brain Cingulate Gyrus	brain
38	chr8:61613600-61615400	Weak transcription	Left Ventricle	heart
39	chr8:61613600-61616200	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr8:61613600-61616800	Enhancers	Brain Hippocampus Middle	brain
41	chr8:61613600-61616800	Weak transcription	Pancreas	Pancrea
42	chr8:61613600-61617800	Enhancers	Brain Anterior Caudate	brain
43	chr8:61613600-61619400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:61613600-61619800	Weak transcription	Stomach Mucosa	stomach
45	chr8:61613600-61620400	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr8:61613600-61620400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:61613600-61621000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:61613600-61621000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr8:61613600-61621000	Weak transcription	Lung	lung
50	chr8:61613800-61615200	Weak transcription	Brain Inferior Temporal Lobe	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links