Variant report

Variant	rs16892656
Chromosome Location	chr5:60888202-60888203
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]
rs10939909	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10939910	1.00[EUR][1000 genomes]
rs10939911	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs1472615	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs16891694	1.00[EUR][1000 genomes]
rs16892657	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs1862564	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs56846569	1.00[EUR][1000 genomes]
rs7700652	1.00[EUR][1000 genomes]
rs7713014	1.00[EUR][1000 genomes]
rs7713560	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7728880	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7733845	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60878400-60895400	Weak transcription	Aorta	Aorta
2	chr5:60879200-60889600	Weak transcription	Pancreas	Pancrea
3	chr5:60887000-60895200	Weak transcription	Brain Hippocampus Middle	brain
4	chr5:60888000-60888400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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