Variant report

Variant	rs13287066
Chromosome Location	chr9:96178967-96178968
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10821123	0.91[CHB][hapmap]
rs10821124	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10992729	0.91[AFR][1000 genomes]
rs12379660	0.85[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes]
rs1351117	0.95[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs2151713	0.89[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs4481672	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7022679	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7870079	0.96[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96176600-96179200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:96178200-96181000	Enhancers	Placenta	Placenta
3	chr9:96178600-96179000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr9:96178800-96179600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast 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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