Variant report

Variant	rs11817171
Chromosome Location	chr10:18360057-18360058
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11813889	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16916829	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16916837	1.00[ASN][1000 genomes]
rs58142633	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7067765	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7090868	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74120203	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18359400-18360800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr10:18359600-18361000	Enhancers	NHEK	skin
3	chr10:18359600-18363000	Enhancers	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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