Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11911379	0.90[EUR][1000 genomes]
rs11911634	0.82[EUR][1000 genomes]
rs11911757	0.90[EUR][1000 genomes]
rs2823320	0.94[EUR][1000 genomes]
rs2823321	0.94[EUR][1000 genomes]
rs2823322	0.93[EUR][1000 genomes]
rs55788196	0.91[EUR][1000 genomes]
rs55817400	0.94[EUR][1000 genomes]
rs55908998	0.92[EUR][1000 genomes]
rs55936117	0.93[EUR][1000 genomes]
rs56174393	0.93[EUR][1000 genomes]
rs57843759	0.90[EUR][1000 genomes]
rs59487397	0.90[EUR][1000 genomes]
rs60282418	0.90[EUR][1000 genomes]
rs60944484	0.91[EUR][1000 genomes]
rs62217401	0.91[EUR][1000 genomes]
rs62217403	0.93[EUR][1000 genomes]
rs62217409	0.93[EUR][1000 genomes]
rs62217411	0.93[EUR][1000 genomes]
rs6517465	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6517467	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6650846	0.92[EUR][1000 genomes]
rs7279689	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7279999	0.95[CEU][hapmap];0.87[TSI][hapmap];0.92[EUR][1000 genomes]
rs7282872	0.92[EUR][1000 genomes]
rs7283918	0.92[EUR][1000 genomes]
rs73187667	0.91[EUR][1000 genomes]
rs73892642	0.92[EUR][1000 genomes]
rs9305646	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9979910	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9984697	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]

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	nsv1063385	chr21:16521617-16926212	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1064280	chr21:16664312-17049272	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv834049	chr21:16717421-16905300	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1064621	chr21:16881027-16937290	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16887400-16893600	Weak transcription	Fetal Thymus	thymus
2	chr21:16887800-16893000	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr21:16887800-16893000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr21:16887800-16893200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr21:16888000-16892800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr21:16888000-16892800	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr21:16888000-16893000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr21:16888200-16893000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr21:16888600-16892800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr21:16888800-16893000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr21:16889000-16893000	Weak transcription	HepG2	liver
12	chr21:16891800-16892200	Weak transcription	Primary T cells from cord blood	blood
13	chr21:16891800-16893400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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