Variant report

Variant	rs61790671
Chromosome Location	chr1:84136967-84136968
allele	C/T
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]
rs10782815	0.89[ASN][1000 genomes]
rs10874404	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10874405	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11590582	0.90[ASN][1000 genomes]
rs11590583	0.90[ASN][1000 genomes]
rs12409454	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4379690	0.90[ASN][1000 genomes]
rs4415589	0.90[ASN][1000 genomes]
rs4548461	0.90[ASN][1000 genomes]
rs7417359	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84136400-84137200	Enhancers	GM12878-XiMat	blood
2	chr1:84136600-84137000	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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