Variant report

Variant	rs17128330
Chromosome Location	chr14:55713145-55713146
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000258413	Chromatin interaction
ENSG00000271180	Chromatin interaction
ENSG00000178974	Chromatin interaction
ENSG00000126775	Chromatin interaction

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

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

rs_ID	r²[population]
rs17128332	0.90[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17128336	0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17128338	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57787897	1.00[EUR][1000 genomes]
rs60824910	1.00[EUR][1000 genomes]
rs61593470	1.00[EUR][1000 genomes]
rs61709162	1.00[EUR][1000 genomes]
rs7140848	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73275722	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8010658	0.81[LWK][hapmap];0.97[MKK][hapmap]

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

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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