Variant report

Variant	rs16869589
Chromosome Location	chr7:71376368-71376369
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10950285	0.82[AMR][1000 genomes]
rs10950286	0.84[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11766067	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11766746	0.89[CHB][hapmap]
rs11767496	0.82[AMR][1000 genomes]
rs11769248	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11772460	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12164040	0.82[AMR][1000 genomes]
rs12537432	0.89[CHB][hapmap]
rs12537492	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs17144059	0.86[JPT][hapmap]
rs17425888	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2051883	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2051884	0.83[ASN][1000 genomes]
rs2158656	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs2867559	0.84[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59392444	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs66607901	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67172404	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6944606	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6946044	0.83[CEU][hapmap];1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs6956808	0.83[ASN][1000 genomes]
rs6956922	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6958157	0.80[AMR][1000 genomes]
rs6961327	0.89[CHB][hapmap]
rs6965098	0.84[CEU][hapmap];1.00[CHB][hapmap];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6967264	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6969870	0.86[JPT][hapmap]
rs726469	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs733909	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7349979	0.85[JPT][hapmap]
rs769022	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7776793	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026896	chr7:71003462-71721516	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1027496	chr7:71162362-71575116	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916220	chr7:71200006-71708048	Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv531372	chr7:71300090-71909517	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	nsv1017367	chr7:71339782-71476575	ZNF genes & repeats Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71375600-71379800	Weak transcription	Thymus	Thymus
2	chr7:71375800-71377000	Enhancers	Fetal Brain Male	brain
3	chr7:71375800-71379600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr7:71375800-71381800	Weak transcription	Fetal Thymus	thymus
5	chr7:71376000-71379200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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