Variant report

Variant	rs28415897
Chromosome Location	chr18:45092356-45092357
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10163590	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10163681	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10163901	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10502884	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1105471	1.00[ASN][1000 genomes]
rs12326663	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17736304	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17736377	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17736432	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1876926	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28379424	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28607937	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28634667	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28702728	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28723450	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4297773	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4536534	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4939746	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4939766	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4940330	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4940345	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4940346	0.86[AFR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57331079	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60405448	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7226723	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72920693	0.82[EUR][1000 genomes]
rs72922530	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72922533	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72922556	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72922557	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73953253	0.93[ASN][1000 genomes]
rs8089178	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8092886	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9946093	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9949386	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9960019	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9960348	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9960587	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9962814	0.87[EUR][1000 genomes]
rs9962920	0.87[EUR][1000 genomes]
rs9963494	0.85[EUR][1000 genomes]
rs9963568	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3317742	chr18:45092079-45093413	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3317743	chr18:45092150-45093325	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45089800-45094000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr18:45090200-45103000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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