Variant report

Variant	rs9497244
Chromosome Location	chr6:145650328-145650329
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	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484968	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497243	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497246	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497248	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497249	1.00[AMR][1000 genomes]
rs9497250	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497253	0.93[YRI][hapmap];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145646000-145652000	Weak transcription	Fetal Heart	heart
2	chr6:145649200-145651200	Enhancers	Stomach Smooth Muscle	stomach
3	chr6:145649200-145652200	Weak transcription	Fetal Muscle Leg	muscle
4	chr6:145649800-145650400	Enhancers	Right Atrium	heart
5	chr6:145650200-145651200	Enhancers	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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