Variant report

Variant	rs2823342
Chromosome Location	chr21:16908241-16908242
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:16907370..16908917-chr21:16935643..16937758,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10854386	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11088441	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11088442	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11088443	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11088447	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11909880	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11911998	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11912014	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12151954	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1556288	0.83[EUR][1000 genomes]
rs2823325	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2823326	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2823333	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2823335	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2823337	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2823347	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2823348	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2823350	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2823352	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2823359	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2823361	0.92[EUR][1000 genomes]
rs4816600	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56116400	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs57533932	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61412083	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61704885	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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	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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16907400-16909400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr21:16907400-16909400	Enhancers	Dnd41	blood
3	chr21:16908200-16911600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr21:16908200-16911800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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