Variant report

Variant	rs2726919
Chromosome Location	chr11:108745652-108745653
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:108743296..108746092-chr11:108747045..108750308,3	K562	blood:
2	chr11:108745387..108747861-chr11:108753103..108755912,2	K562	blood:

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10502103	0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs10749925	0.85[CEU][hapmap];0.85[CHB][hapmap]
rs12574567	0.85[CHB][hapmap]
rs12574721	0.90[CHB][hapmap];0.82[ASN][1000 genomes]
rs12574758	0.82[ASN][1000 genomes]
rs12575278	0.81[CHB][hapmap]
rs12577382	0.82[ASN][1000 genomes]
rs12785398	0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs12794048	0.85[CHB][hapmap]
rs12794597	0.81[ASN][1000 genomes]
rs12796331	0.85[CHB][hapmap]
rs12800516	0.85[CHB][hapmap]
rs12800726	0.85[CHB][hapmap]
rs12801974	0.85[CHB][hapmap]
rs12802313	0.85[CHB][hapmap];0.82[ASN][1000 genomes]
rs12808060	0.85[CHB][hapmap]
rs12808674	0.82[ASN][1000 genomes]
rs1365046	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1365047	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1365048	1.00[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17108571	0.80[CHB][hapmap]
rs17108703	0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs17108744	0.82[CHB][hapmap]
rs2042677	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2042678	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2061681	0.85[CEU][hapmap]
rs2553749	0.85[CHB][hapmap]
rs2553750	0.85[CHB][hapmap]
rs2553751	0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs2553754	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2553757	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2553758	1.00[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2553760	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2553761	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2615725	0.85[CEU][hapmap]
rs2615727	0.86[CEU][hapmap];0.85[CHB][hapmap]
rs2615756	0.83[CEU][hapmap];0.83[ASN][1000 genomes]
rs2726885	0.85[CHB][hapmap]
rs2726886	0.85[CEU][hapmap]
rs2726896	0.85[CHB][hapmap]
rs2726907	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2726908	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2726910	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2726911	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2726913	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2726914	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2726915	1.00[CEU][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2726916	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2726920	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34350110	0.82[ASN][1000 genomes]
rs34354308	0.82[ASN][1000 genomes]
rs35244070	0.82[ASN][1000 genomes]
rs35430545	0.82[ASN][1000 genomes]
rs4497371	0.89[YRI][hapmap]
rs57014838	0.81[ASN][1000 genomes]
rs71489925	0.82[ASN][1000 genomes]
rs898972	0.85[CHB][hapmap];0.82[ASN][1000 genomes]
rs970162	0.85[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052254	chr11:108122683-108845008	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv541164	chr11:108122683-108845008	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv898386	chr11:108409442-108831875	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv898389	chr11:108724639-108891986	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108726200-108768400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr11:108728400-108810600	Weak transcription	Left Ventricle	heart
3	chr11:108734600-108753200	Weak transcription	GM12878-XiMat	blood
4	chr11:108741800-108750400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:108741800-108756600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:108742400-108753400	Weak transcription	Ovary	ovary
7	chr11:108743800-108746600	Enhancers	NH-A	brain
8	chr11:108744000-108746200	Enhancers	HUVEC	blood vessel
9	chr11:108744000-108754000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:108744200-108746200	Enhancers	Muscle Satellite Cultured Cells	--
11	chr11:108744200-108746200	Weak transcription	HMEC	breast
12	chr11:108744200-108751200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:108744400-108745800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:108744400-108746200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr11:108744600-108745800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr11:108744800-108746200	Enhancers	Osteobl	bone
17	chr11:108744800-108751200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr11:108744800-108754800	Weak transcription	HSMM	muscle
19	chr11:108745200-108746000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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