Variant report

Variant	rs7001687
Chromosome Location	chr8:64746201-64746202
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10091619	0.87[EUR][1000 genomes]
rs10102099	0.92[ASN][1000 genomes]
rs1025161	0.92[ASN][1000 genomes]
rs10481236	0.92[ASN][1000 genomes]
rs13262007	0.93[ASN][1000 genomes]
rs13278212	0.93[ASN][1000 genomes]
rs1425602	0.93[ASN][1000 genomes]
rs1425608	0.93[ASN][1000 genomes]
rs1520933	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.87[EUR][1000 genomes]
rs16930736	0.92[ASN][1000 genomes]
rs1963375	0.92[ASN][1000 genomes]
rs2081481	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28470645	0.90[ASN][1000 genomes]
rs28526535	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7837125	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7837174	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[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	chr8:64746000-64746400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr8:64746200-64746400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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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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