Variant report

Variant	rs8051376
Chromosome Location	chr16:71295114-71295115
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10500556	1.00[AMR][1000 genomes]
rs11859416	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11861972	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11863110	0.91[YRI][hapmap]
rs16970857	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16973164	1.00[AMR][1000 genomes]
rs2004142	1.00[AMR][1000 genomes]
rs2040652	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2158104	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56996503	1.00[AMR][1000 genomes]
rs59737920	1.00[AMR][1000 genomes]
rs60009511	1.00[AMR][1000 genomes]
rs61559998	1.00[AMR][1000 genomes]
rs7202726	1.00[AMR][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	esv2758429	chr16:70807122-71316983	Active TSS ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	esv2758653	chr16:70807122-71316983	Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv949461	chr16:71196153-71579711	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
4	nsv482374	chr16:71228600-71401617	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1860	chr16:71269156-71313852	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71290200-71317200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr16:71291800-71296400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr16:71292200-71295200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr16:71292400-71295400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr16:71292800-71297400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr16:71294800-71295200	Enhancers	Brain Cingulate Gyrus	brain
7	chr16:71295000-71297600	Enhancers	Brain Germinal Matrix	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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