Variant report

Variant	rs8009718
Chromosome Location	chr14:55717379-55717380
allele	A/G
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]
rs10139912	0.94[EUR][1000 genomes]
rs11845284	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17742621	0.83[CEU][hapmap]
rs2274271	0.86[CHB][hapmap];0.87[CHD][hapmap];0.83[JPT][hapmap];0.82[MEX][hapmap]
rs28837432	0.82[ASN][1000 genomes]
rs7141706	0.82[EUR][1000 genomes]
rs7160411	0.86[TSI][hapmap]
rs8009244	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8012397	0.86[TSI][hapmap]
rs8013528	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55717200-55717400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:55717200-55717600	Bivalent Enhancer	Esophagus	oesophagus

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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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