Variant report

Variant	rs899612
Chromosome Location	chr7:146996755-146996756
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:146989620..146992429-chr7:146994596..146997108,3	K562	blood:

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10085764	0.93[YRI][hapmap]
rs1021008	0.85[CHB][hapmap]
rs10225100	0.85[CHB][hapmap];0.93[YRI][hapmap]
rs10234386	0.82[CHB][hapmap];0.80[YRI][hapmap]
rs10238730	0.82[YRI][hapmap]
rs10242430	0.93[YRI][hapmap]
rs10248220	0.89[CHB][hapmap]
rs10251412	0.91[YRI][hapmap]
rs10261539	0.84[CHB][hapmap]
rs10261547	0.89[CHB][hapmap];0.94[JPT][hapmap]
rs10262107	0.92[YRI][hapmap]
rs10808044	0.85[CHB][hapmap];0.89[YRI][hapmap]
rs10952678	0.82[CHB][hapmap];0.93[YRI][hapmap];0.82[AFR][1000 genomes]
rs12531764	0.85[CHB][hapmap];0.86[YRI][hapmap]
rs12534978	0.81[CHB][hapmap]
rs12703895	0.82[CHB][hapmap];0.93[YRI][hapmap];0.83[AFR][1000 genomes]
rs12703900	0.81[YRI][hapmap]
rs13235260	0.82[CHB][hapmap]
rs1383011	0.82[CHB][hapmap]
rs1404703	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs1404706	0.89[ASN][1000 genomes]
rs1404707	0.85[CHB][hapmap]
rs1479837	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1479838	0.85[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1479839	0.89[ASN][1000 genomes]
rs1479840	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1525208	0.89[ASN][1000 genomes]
rs1525209	0.85[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1525210	0.89[ASN][1000 genomes]
rs1525211	0.82[CHB][hapmap];0.97[YRI][hapmap]
rs1525215	0.85[CHB][hapmap]
rs1525216	0.85[CHB][hapmap]
rs1917600	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs2373026	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2620439	0.85[CHB][hapmap];0.83[YRI][hapmap]
rs2620440	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2620441	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2620443	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2620446	0.86[CHB][hapmap];0.94[JPT][hapmap]
rs2620447	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2620450	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2620452	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2620454	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs2620455	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2620460	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2620464	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs2620465	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs2620467	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs2692139	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2692140	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2692141	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2692143	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2692144	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2692145	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2692146	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2692149	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs2692150	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2692151	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2692154	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2692157	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs2692158	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2692162	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2692163	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2692164	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2692168	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2692170	0.89[ASN][1000 genomes]
rs2692173	0.89[ASN][1000 genomes]
rs2692174	0.89[ASN][1000 genomes]
rs2692175	0.85[ASN][1000 genomes]
rs2692176	0.95[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs2692177	0.89[ASN][1000 genomes]
rs2692178	0.89[ASN][1000 genomes]
rs2692179	0.85[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2692180	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2692182	0.94[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs2692183	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2692185	0.83[JPT][hapmap]
rs2692186	0.97[YRI][hapmap]
rs2692187	0.82[CHB][hapmap];0.90[YRI][hapmap]
rs34748606	0.81[AFR][1000 genomes]
rs4269450	1.00[JPT][hapmap]
rs6974852	0.82[CHB][hapmap]
rs728720	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs899613	0.95[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs899614	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs899615	0.95[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs899616	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9969115	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs9969256	0.85[CHB][hapmap];1.00[JPT][hapmap]

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	nsv933033	chr7:146720301-147081560	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1033898	chr7:146721499-147081768	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv889396	chr7:146854133-147035067	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1026360	chr7:146988190-147012081	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv1033398	chr7:146989035-147101573	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	n/a
7	nsv1029946	chr7:146993413-147021947	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146996400-146997000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:146996400-146998800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:146996400-147000000	Weak transcription	Fetal Muscle Leg	muscle
4	chr7:146996400-147000800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:146996400-147000800	Weak transcription	Fetal Lung	lung
6	chr7:146996400-147008000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr7:146996600-147000800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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