Variant report

Variant	rs4649943
Chromosome Location	chr1:72232842-72232843
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10789328	0.92[EUR][1000 genomes]
rs10789330	0.92[EUR][1000 genomes]
rs11209818	0.92[JPT][hapmap]
rs11209837	0.91[EUR][1000 genomes]
rs11209840	0.85[EUR][1000 genomes]
rs11209841	0.88[CEU][hapmap];0.92[JPT][hapmap]
rs11209842	0.88[CEU][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes]
rs11209844	0.82[CEU][hapmap];0.94[CHB][hapmap];0.91[JPT][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11578097	0.90[JPT][hapmap]
rs11584866	0.90[JPT][hapmap]
rs1158573	0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11588321	0.83[JPT][hapmap]
rs12023733	0.82[JPT][hapmap]
rs12024388	0.90[JPT][hapmap]
rs12030035	0.83[JPT][hapmap]
rs12031657	0.82[JPT][hapmap]
rs12031842	0.81[JPT][hapmap]
rs12037107	0.92[JPT][hapmap]
rs12040327	0.90[JPT][hapmap]
rs12041607	0.82[JPT][hapmap]
rs12043796	0.83[JPT][hapmap]
rs12048869	0.90[JPT][hapmap]
rs12731898	0.92[EUR][1000 genomes]
rs1459795	0.92[EUR][1000 genomes]
rs1491198	0.90[JPT][hapmap]
rs1591382	0.82[JPT][hapmap]
rs1599179	0.89[CEU][hapmap];0.92[EUR][1000 genomes]
rs17091704	0.90[JPT][hapmap]
rs17091710	0.90[JPT][hapmap]
rs1817805	0.92[EUR][1000 genomes]
rs1844788	0.91[EUR][1000 genomes]
rs1870523	0.89[CEU][hapmap];0.91[JPT][hapmap];0.92[EUR][1000 genomes]
rs1870524	0.91[EUR][1000 genomes]
rs1870525	0.88[CEU][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes]
rs2061495	0.92[EUR][1000 genomes]
rs2125775	0.89[CEU][hapmap];0.91[JPT][hapmap];0.92[EUR][1000 genomes]
rs2125776	0.88[CEU][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes]
rs2125777	0.88[CEU][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes]
rs2169096	0.92[EUR][1000 genomes]
rs4649945	0.89[CEU][hapmap];0.81[CHB][hapmap];0.92[JPT][hapmap];0.92[EUR][1000 genomes]
rs4649947	0.88[CEU][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes]
rs4649949	0.91[JPT][hapmap]
rs4649950	0.92[JPT][hapmap]
rs4650121	0.92[EUR][1000 genomes]
rs4650122	0.91[EUR][1000 genomes]
rs4650123	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs482060	0.88[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs497074	1.00[YRI][hapmap]
rs531071	1.00[YRI][hapmap]
rs6424448	0.90[JPT][hapmap]
rs6671557	0.81[JPT][hapmap]
rs6697370	0.92[JPT][hapmap]
rs6701156	0.82[JPT][hapmap]
rs7520452	0.89[EUR][1000 genomes]
rs7528030	0.92[JPT][hapmap]
rs7531512	0.82[JPT][hapmap]
rs9662397	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949599	chr1:71655652-72327802	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1007250	chr1:71998391-72350683	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv534992	chr1:71998391-72350683	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv948821	chr1:72049987-72477221	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1003446	chr1:72060680-72419918	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv461884	chr1:72077549-72238691	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv546476	chr1:72077549-72238691	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv817447	chr1:72098815-72558020	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1008210	chr1:72099161-72374197	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv533779	chr1:72124095-72241965	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv830181	chr1:72155983-72296578	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv916783	chr1:72196061-72707953	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr1:72232400-72233000	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr1:72232400-72233800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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