Variant report

Variant	rs11974322
Chromosome Location	chr7:40634315-40634316
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:40633290..40635892-chr7:40636595..40638399,2	K562	blood:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs1000013	1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1019018	1.00[CEU][hapmap];1.00[JPT][hapmap];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10254954	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10256576	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs10263677	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10429076	1.00[ASN][1000 genomes]
rs10486810	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10486811	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11973006	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11977013	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11980464	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11982075	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17171727	1.00[CEU][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17171730	1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs17171734	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs17171747	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1859660	1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1859705	0.84[ASN][1000 genomes]
rs2329818	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs2329819	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28657711	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34523428	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs3919491	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs4720368	0.80[EUR][1000 genomes]
rs4720370	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs4720371	1.00[CEU][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4723966	0.80[EUR][1000 genomes]
rs4723967	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4723968	0.80[EUR][1000 genomes]
rs4723969	0.80[EUR][1000 genomes]
rs4723970	0.84[EUR][1000 genomes]
rs4723972	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60011074	0.89[EUR][1000 genomes]
rs60999211	0.91[EUR][1000 genomes]
rs61107746	0.97[ASN][1000 genomes]
rs6462985	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67340458	1.00[ASN][1000 genomes]
rs6943787	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6945570	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6948724	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6948900	1.00[JPT][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6954401	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6956277	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6977104	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73122188	1.00[ASN][1000 genomes]
rs73308254	0.80[EUR][1000 genomes]
rs73308257	0.80[EUR][1000 genomes]
rs73308260	0.84[EUR][1000 genomes]
rs73308263	0.84[EUR][1000 genomes]
rs73308264	0.86[EUR][1000 genomes]
rs73308269	0.85[EUR][1000 genomes]
rs73308281	0.90[EUR][1000 genomes]
rs73308284	0.89[EUR][1000 genomes]
rs73308289	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73308291	0.91[EUR][1000 genomes]
rs73308300	0.91[EUR][1000 genomes]
rs73310208	0.94[EUR][1000 genomes]
rs7459324	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs7808612	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs917204	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9632613	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030648	chr7:40218618-41032599	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1030515	chr7:40501867-40634808	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv887987	chr7:40505382-40748650	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv830971	chr7:40523075-40700172	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1025605	chr7:40623026-40789063	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv538823	chr7:40623026-40789063	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40630800-40637600	Weak transcription	Aorta	Aorta
2	chr7:40634200-40634400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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