Variant report

Variant	rs1435064
Chromosome Location	chr3:191019005-191019006
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10937468	0.80[JPT][hapmap]
rs10937470	0.81[JPT][hapmap]
rs10937471	0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs10937472	0.95[ASN][1000 genomes]
rs10937473	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10937474	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10937475	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11720878	0.95[ASN][1000 genomes]
rs11720880	0.95[ASN][1000 genomes]
rs1195560	0.90[ASN][1000 genomes]
rs1195561	0.91[ASN][1000 genomes]
rs12486272	0.95[ASN][1000 genomes]
rs12488393	0.95[ASN][1000 genomes]
rs12490850	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12495011	0.95[ASN][1000 genomes]
rs12495014	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12496729	0.95[ASN][1000 genomes]
rs12631157	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12638308	0.95[ASN][1000 genomes]
rs12638950	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13067368	0.95[ASN][1000 genomes]
rs13078168	0.95[ASN][1000 genomes]
rs1369280	0.95[ASN][1000 genomes]
rs1398717	0.95[ASN][1000 genomes]
rs1398718	0.95[ASN][1000 genomes]
rs1435065	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1435066	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs150503	0.98[ASN][1000 genomes]
rs1584935	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1594950	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs184142	0.98[ASN][1000 genomes]
rs2117544	0.95[ASN][1000 genomes]
rs2117545	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2117546	0.95[ASN][1000 genomes]
rs2117547	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2572061	0.87[ASN][1000 genomes]
rs293863	0.98[ASN][1000 genomes]
rs293866	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs293867	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs297390	0.96[EUR][1000 genomes]
rs34670047	0.93[ASN][1000 genomes]
rs55661359	0.90[ASN][1000 genomes]
rs6444532	0.82[CEU][hapmap]
rs6444533	0.80[JPT][hapmap]
rs6765280	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6765783	0.95[ASN][1000 genomes]
rs6769894	0.94[ASN][1000 genomes]
rs6769898	0.95[ASN][1000 genomes]
rs6769915	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67775561	0.93[ASN][1000 genomes]
rs6786046	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6788097	0.81[JPT][hapmap]
rs6788319	0.81[JPT][hapmap]
rs6794234	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6796119	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6801672	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6801766	0.95[ASN][1000 genomes]
rs7645540	0.80[JPT][hapmap]
rs9835846	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9854723	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428100	chr3:190793797-191092633	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv931943	chr3:190860224-191321873	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv2757910	chr3:190867011-191279107	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers 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	12 gene(s)	inside rSNPs	diseases
4	esv2759209	chr3:190867011-191279107	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv878101	chr3:190891939-191059322	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv428428	chr3:190936834-191215596	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv997716	chr3:190943706-191027499	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:191010200-191021000	Enhancers	Primary B cells from peripheral blood	blood
2	chr3:191015600-191019600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:191017200-191019800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:191018400-191019200	Flanking Active TSS	GM12878-XiMat	blood
5	chr3:191018600-191019200	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr3:191018600-191019600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr3:191018600-191019800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr3:191018800-191020400	Enhancers	Primary B cells from cord blood	blood
9	chr3:191019000-191019400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr3:191019000-191020000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:191019000-191020800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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