Variant report

Variant	rs256592
Chromosome Location	chr16:52101509-52101510
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs256597	0.80[YRI][hapmap]
rs33337	1.00[AMR][1000 genomes]
rs33338	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs40498	1.00[YRI][hapmap];1.00[AMR][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	nsv492248	chr16:51681902-52456082	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	esv34024	chr16:51878565-52316530	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv827650	chr16:52067728-52124369	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv1058257	chr16:52093549-52271815	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:52101000-52102000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr16:52101200-52101600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr16:52101200-52101600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr16:52101200-52101600	Flanking Active TSS	Brain Hippocampus Middle	brain
5	chr16:52101200-52101600	Enhancers	Duodenum Smooth Muscle	Duodenum
6	chr16:52101200-52102400	Enhancers	Brain Cingulate Gyrus	brain
7	chr16:52101200-52102400	Enhancers	Brain Substantia Nigra	brain
8	chr16:52101200-52102600	Enhancers	Brain Anterior Caudate	brain
9	chr16:52101200-52102600	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr16:52101400-52102000	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr16:52101400-52102400	Enhancers	Brain Angular Gyrus	brain
12	chr16:52101400-52110400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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