Variant report

Variant	rs6884436
Chromosome Location	chr5:151235182-151235183
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs17112284	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56660412	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59477412	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs59891102	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs61271148	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6860343	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6889290	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6896784	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs73285976	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7706897	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7707162	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7707359	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151231200-151242800	Weak transcription	Aorta	Aorta
2	chr5:151233800-151235200	Strong transcription	Pancreatic Islets	Pancreatic Islet

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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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