Variant report

Variant	rs72779435
Chromosome Location	chr5:94431662-94431663
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]
rs11960770	1.00[ASN][1000 genomes]
rs72779406	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72779407	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72779408	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72779410	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72779411	0.83[EUR][1000 genomes]
rs72779424	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72779429	0.93[ASN][1000 genomes]
rs72779434	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72779437	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs890294	0.82[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94431400-94433600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:94431600-94432600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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