Variant report

Variant	rs6987331
Chromosome Location	chr8:121691595-121691596
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11783798	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11992540	1.00[YRI][hapmap]
rs11993445	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12235050	1.00[YRI][hapmap]
rs34245253	0.93[ASN][1000 genomes]
rs35780243	0.93[ASN][1000 genomes]
rs4076711	0.80[CHB][hapmap];0.95[JPT][hapmap];0.85[TSI][hapmap];0.82[ASN][1000 genomes]
rs4077726	0.80[CHB][hapmap];0.95[JPT][hapmap];0.85[TSI][hapmap];0.82[ASN][1000 genomes]
rs4077727	0.82[ASN][1000 genomes]
rs4307384	0.89[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4360333	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4361791	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4366115	0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs4392948	0.80[CHB][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.85[TSI][hapmap];0.82[ASN][1000 genomes]
rs4512418	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4515598	0.82[ASN][1000 genomes]
rs4607661	0.82[ASN][1000 genomes]
rs4870742	0.89[CHB][hapmap];0.80[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4871092	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4871093	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs5003013	0.80[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs59486364	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6469944	0.82[ASN][1000 genomes]
rs66856703	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6986798	0.80[CHB][hapmap];0.95[JPT][hapmap];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6987352	0.90[JPT][hapmap];0.85[TSI][hapmap];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7828909	0.80[CHB][hapmap];0.95[JPT][hapmap];0.85[TSI][hapmap];0.82[ASN][1000 genomes]
rs7837985	0.80[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs7842679	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv6369	chr8:121654665-121699920	ZNF genes & repeats Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1016172	chr8:121679590-121929916	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv891422	chr8:121680857-121819478	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121672600-121699600	Weak transcription	HSMM	muscle
2	chr8:121679800-121714600	Weak transcription	Spleen	Spleen
3	chr8:121680600-121697600	Weak transcription	Gastric	stomach
4	chr8:121680600-121704600	Weak transcription	Fetal Intestine Large	intestine
5	chr8:121680800-121701000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr8:121681400-121704200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr8:121681600-121699600	Weak transcription	Osteobl	bone
8	chr8:121681600-121701000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr8:121682200-121700400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr8:121682800-121698000	Weak transcription	Primary B cells from cord blood	blood
11	chr8:121685400-121697200	Weak transcription	Lung	lung
12	chr8:121685400-121714400	Weak transcription	Pancreas	Pancrea
13	chr8:121685600-121714200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr8:121686200-121697200	Weak transcription	Fetal Muscle Trunk	muscle
15	chr8:121686200-121697600	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr8:121686600-121704400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr8:121686800-121695800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr8:121686800-121696400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:121686800-121697200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr8:121686800-121709000	Weak transcription	Small Intestine	intestine
21	chr8:121687000-121697600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr8:121687000-121704200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr8:121688200-121699600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:121688200-121699600	Weak transcription	NHLF	lung
25	chr8:121688200-121701000	Weak transcription	Psoas Muscle	Psoas
26	chr8:121689800-121691800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr8:121690000-121691600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr8:121690200-121706600	Strong transcription	HepG2	liver
29	chr8:121690600-121699200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:121690800-121695600	Weak transcription	Primary T cells from cord blood	blood
31	chr8:121690800-121697200	Weak transcription	Fetal Stomach	stomach
32	chr8:121690800-121699600	Weak transcription	HSMMtube	muscle
33	chr8:121691000-121696200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr8:121691200-121692600	Weak transcription	Liver	Liver
35	chr8:121691200-121693400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr8:121691200-121697200	Weak transcription	Fetal Muscle Leg	muscle
37	chr8:121691200-121703600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:121691400-121692200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr8:121691400-121694600	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr8:121691400-121697000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr8:121691400-121698200	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr8:121691400-121705200	Weak transcription	Sigmoid Colon	Sigmoid Colon

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