Variant report

Variant	rs34755428
Chromosome Location	chr5:90909635-90909636
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs13161413	0.82[EUR][1000 genomes]
rs13169804	0.82[EUR][1000 genomes]
rs2062965	0.82[EUR][1000 genomes]
rs34444727	0.82[EUR][1000 genomes]
rs34556970	0.82[EUR][1000 genomes]
rs71637341	0.82[EUR][1000 genomes]
rs71637348	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs71637349	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034732	chr5:90834465-90925707	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90907600-90909800	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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