Variant report

Variant	rs4355554
Chromosome Location	chr5:90935334-90935335
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10071476	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1566996	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2202508	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2657819	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2962380	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35013513	0.87[EUR][1000 genomes]
rs35662958	0.86[EUR][1000 genomes]
rs36016458	0.92[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90934200-90940400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:90934600-90936600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:90935200-90936400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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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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