Variant report

Variant	rs35539975
Chromosome Location	chr5:91607148-91607149
allele	A/G
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]
rs12697832	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34624654	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4279370	0.83[ASN][1000 genomes]
rs4403206	0.82[ASN][1000 genomes]
rs6867657	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72777009	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72777045	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7446138	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7703201	0.81[ASN][1000 genomes]
rs7720274	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7724444	0.81[AMR][1000 genomes]
rs7728271	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7728797	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7730246	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9293606	0.81[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91604000-91607200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:91604000-91607200	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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