Variant report

Variant	rs9450799
Chromosome Location	chr6:88469981-88469982
allele	C/G
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]
rs9444523	1.00[EUR][1000 genomes]
rs9444545	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9444546	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9444547	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9444548	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9450784	1.00[EUR][1000 genomes]
rs9450789	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9450791	1.00[EUR][1000 genomes]
rs9450794	1.00[AFR][1000 genomes]
rs9450796	1.00[AFR][1000 genomes]
rs9450797	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9450798	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9450803	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:88457800-88482400	Weak transcription	Placenta	Placenta
2	chr6:88466800-88472000	Weak transcription	Spleen	Spleen
3	chr6:88467000-88470000	Enhancers	GM12878-XiMat	blood
4	chr6:88467000-88475800	Weak transcription	Fetal Lung	lung
5	chr6:88467400-88470400	Weak transcription	HepG2	liver

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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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