Variant report

Variant	rs8092757
Chromosome Location	chr18:45088519-45088520
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11082608	0.87[EUR][1000 genomes]
rs11082609	0.88[EUR][1000 genomes]
rs1108794	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1510014	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16954613	0.90[EUR][1000 genomes]
rs16954994	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59194254	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6507765	0.83[EUR][1000 genomes]
rs7230633	0.88[EUR][1000 genomes]
rs7236741	0.85[EUR][1000 genomes]
rs7505509	0.82[EUR][1000 genomes]
rs8090686	0.89[EUR][1000 genomes]
rs8094987	0.83[EUR][1000 genomes]
rs8095159	0.80[EUR][1000 genomes]
rs8096375	0.85[EUR][1000 genomes]
rs880876	0.81[EUR][1000 genomes]

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45086200-45088600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr18:45086400-45088600	Enhancers	H1 Cell Line	embryonic stem cell
3	chr18:45086600-45088600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr18:45086600-45089000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr18:45086600-45089000	Enhancers	Brain Germinal Matrix	brain
6	chr18:45087800-45088600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr18:45088200-45088600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr18:45088200-45088800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr18:45088200-45088800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr18:45088400-45088600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr18:45088400-45088600	Enhancers	iPS DF 19.11 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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