Variant report

Variant	rs17007809
Chromosome Location	chr1:220654645-220654646
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10047144	1.00[MEX][hapmap]
rs10047220	1.00[MEX][hapmap]
rs12408093	1.00[MEX][hapmap]
rs17007786	0.91[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17007798	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57150991	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59319544	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59822514	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61161249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61406326	1.00[AMR][1000 genomes]
rs7543744	1.00[AMR][1000 genomes]
rs7543764	1.00[AMR][1000 genomes]
rs7553213	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220653800-220656600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:220654000-220656600	Weak transcription	Adipose Nuclei	Adipose

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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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