Variant report

Variant	rs9497250
Chromosome Location	chr6:145654919-145654920
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10223396	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484968	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497243	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497244	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497246	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497248	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497249	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497253	1.00[YRI][hapmap];0.81[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	chr6:145654800-145655000	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr6:145654800-145655000	Enhancers	iPS-15b 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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