Variant report

Variant	rs9475655
Chromosome Location	chr6:56150981-56150982
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10223442	1.00[ASN][1000 genomes]
rs12208321	1.00[ASN][1000 genomes]
rs4128442	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62411895	1.00[ASN][1000 genomes]
rs6903416	1.00[ASN][1000 genomes]
rs6917061	1.00[ASN][1000 genomes]
rs72866945	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72870219	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72879914	1.00[ASN][1000 genomes]
rs9475648	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	chr6:56143600-56156200	Weak transcription	Fetal Lung	lung
2	chr6:56143800-56156200	Weak transcription	Colon Smooth Muscle	Colon

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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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