Variant report

Variant	rs17585302
Chromosome Location	chr12:43387272-43387273
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12317369	0.83[EUR][1000 genomes]
rs1520819	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17092544	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17513656	1.00[ASW][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap]
rs2043552	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4768031	0.81[EUR][1000 genomes]
rs4768472	1.00[CEU][hapmap];1.00[GIH][hapmap];0.85[EUR][1000 genomes]
rs7955263	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs7958072	1.00[CEU][hapmap];1.00[GIH][hapmap];0.83[EUR][1000 genomes]
rs7968365	1.00[CEU][hapmap];0.89[GIH][hapmap];0.83[EUR][1000 genomes]
rs7968724	1.00[CEU][hapmap];0.85[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:43386800-43387400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:43387200-43387400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:43387200-43387400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:43387200-43387600	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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