Variant report

Variant	rs851701
Chromosome Location	chr7:147487632-147487633
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10282687	1.00[MEX][hapmap]
rs11975355	1.00[EUR][1000 genomes]
rs11977877	1.00[EUR][1000 genomes]
rs12113621	1.00[MEX][hapmap]
rs1525256	1.00[MEX][hapmap]
rs6974353	1.00[MEX][hapmap]
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]
rs851670	1.00[EUR][1000 genomes]
rs851692	0.84[YRI][hapmap]
rs851693	0.90[YRI][hapmap]
rs851695	0.95[YRI][hapmap]

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:0 , 50 per page) page:

No data

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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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