Variant report

Variant	rs851670
Chromosome Location	chr7:147500735-147500736
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:8)

rs_ID	r²[population]
rs11975355	1.00[EUR][1000 genomes]
rs11977877	1.00[EUR][1000 genomes]
rs73462197	1.00[EUR][1000 genomes]
rs73464209	1.00[EUR][1000 genomes]
rs73464229	1.00[EUR][1000 genomes]
rs73464231	1.00[EUR][1000 genomes]
rs7785335	1.00[EUR][1000 genomes]
rs851667	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933973	chr7:147438206-147549993	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
2	nsv889397	chr7:147471710-147585819	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147494600-147506200	Weak transcription	Brain Substantia Nigra	brain
2	chr7:147500200-147501600	Enhancers	Fetal Lung	lung
3	chr7:147500400-147500800	Enhancers	Fetal Stomach	stomach
4	chr7:147500400-147501000	Enhancers	Ovary	ovary
5	chr7:147500400-147501600	Enhancers	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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