Variant report

Variant	rs12482106
Chromosome Location	chr21:16637260-16637261
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1018354	0.84[AMR][1000 genomes]
rs12481765	0.91[AMR][1000 genomes]
rs12482240	0.91[AMR][1000 genomes]
rs12482854	0.91[AMR][1000 genomes]
rs12483327	0.86[AMR][1000 genomes]
rs1304524	1.00[JPT][hapmap]
rs17275030	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2823199	1.00[JPT][hapmap]
rs62220260	1.00[ASN][1000 genomes]
rs62220261	1.00[ASN][1000 genomes]
rs62220262	1.00[ASN][1000 genomes]
rs969146	1.00[JPT][hapmap];0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16632800-16641600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr21:16636200-16653200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr21:16636400-16637400	Weak transcription	Brain Germinal Matrix	brain
4	chr21:16636800-16642000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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

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