Variant report

Variant	rs4939862
Chromosome Location	chr18:45034102-45034103
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs12607893	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2036798	0.82[ASN][1000 genomes]
rs4939854	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7506616	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8095913	0.98[ASN][1000 genomes]
rs9635948	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45033400-45034200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr18:45033800-45035400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr18:45034000-45034400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr18:45034000-45035000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr18:45034000-45036400	Enhancers	ES-UCSF4 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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