Variant report

Variant	rs17093707
Chromosome Location	chr10:117645612-117645613
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1038171	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs12268922	1.00[EUR][1000 genomes]
rs17093701	1.00[EUR][1000 genomes]
rs17093704	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17093727	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17093761	1.00[EUR][1000 genomes]
rs1984757	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2253684	1.00[EUR][1000 genomes]
rs2253786	1.00[EUR][1000 genomes]
rs2615883	1.00[EUR][1000 genomes]
rs2620963	1.00[EUR][1000 genomes]
rs2927372	1.00[EUR][1000 genomes]
rs2927374	1.00[EUR][1000 genomes]
rs7474865	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs922597	1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117634000-117657800	Weak transcription	Aorta	Aorta
2	chr10:117644800-117645800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr10:117645600-117645800	Enhancers	H9 Derived Neuronal Progenitor 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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