Variant report

Variant	rs10502886
Chromosome Location	chr18:45172436-45172437
allele	A/G
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:18)

rs_ID	r²[population]
rs16956000	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28375235	0.82[AFR][1000 genomes]
rs28444636	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28650034	0.82[AFR][1000 genomes]
rs56330224	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57391572	0.85[AFR][1000 genomes]
rs7227134	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7242884	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs7244405	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73953281	0.91[AFR][1000 genomes]
rs8088535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9945915	0.94[AFR][1000 genomes]
rs9946150	0.92[AFR][1000 genomes]
rs9948880	0.92[AFR][1000 genomes]
rs9956762	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9961540	0.94[YRI][hapmap]
rs9961544	0.94[YRI][hapmap]
rs9963571	0.93[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45170800-45173200	Weak transcription	H9 Cell Line	embryonic stem cell

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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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