Variant report

Variant	rs9497246
Chromosome Location	chr6:145653813-145653814
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	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484968	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497243	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497244	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497248	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497249	1.00[AMR][1000 genomes]
rs9497250	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497253	0.92[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145652000-145654000	Enhancers	Fetal Heart	heart
2	chr6:145652600-145654000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr6:145653400-145654800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:145653800-145654800	Weak transcription	HUES6 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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