Variant report

Variant	rs56802057
Chromosome Location	chr10:95563417-95563418
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11187730	1.00[EUR][1000 genomes]
rs11187763	1.00[EUR][1000 genomes]
rs12247837	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12257577	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12267874	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57561176	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60278384	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7079464	1.00[EUR][1000 genomes]
rs7912666	1.00[EUR][1000 genomes]
rs7915843	1.00[EUR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:95552600-95563600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr10:95556200-95563600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr10:95557400-95566600	Weak transcription	Brain Anterior Caudate	brain
4	chr10:95563200-95564400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr10:95563400-95564600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr10:95563400-95564600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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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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