Variant report

Variant	rs17865431
Chromosome Location	chr7:126967239-126967240
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs17864966	1.00[AMR][1000 genomes]
rs17864995	1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs17865398	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17865485	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs17865902	1.00[MEX][hapmap]
rs17866182	0.90[AFR][1000 genomes]
rs17867074	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17869283	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs17869348	0.87[YRI][hapmap]
rs17869705	1.00[AMR][1000 genomes]
rs17875094	1.00[YRI][hapmap];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126967000-126967800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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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