Variant report

Variant	rs7669246
Chromosome Location	chr4:78031867-78031868
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11737413	0.84[ASN][1000 genomes]
rs57011953	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57498549	0.88[ASN][1000 genomes]
rs60645850	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72860237	0.87[ASN][1000 genomes]
rs72860254	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72860266	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72860268	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72860270	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7669540	1.00[ASN][1000 genomes]
rs7699175	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78031800-78032200	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr4:78031800-78032800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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