Variant report

Variant	rs17557498
Chromosome Location	chr6:120286642-120286643
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1028961	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11153850	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12526302	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12528425	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17081699	0.82[EUR][1000 genomes]
rs1751882	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17555372	0.82[EUR][1000 genomes]
rs17557428	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17636773	0.84[EUR][1000 genomes]
rs17637543	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2357764	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35511616	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4945651	0.82[EUR][1000 genomes]
rs4945652	0.83[EUR][1000 genomes]
rs4945653	0.86[EUR][1000 genomes]
rs505838	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs547922	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55673748	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55928287	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56052650	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56074031	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56198187	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56217823	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56320026	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56363464	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57283891	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57334041	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs579071	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs58499424	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58870997	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59614059	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61328226	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs66531327	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs66631049	0.86[EUR][1000 genomes]
rs66665303	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs66912712	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67106263	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67457989	0.86[EUR][1000 genomes]
rs67618941	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67620102	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs67658298	0.86[EUR][1000 genomes]
rs68027538	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs724554	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs726178	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72952828	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72952889	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72954710	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72954771	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7746191	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7761121	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9489858	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9489859	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9489860	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs979327	0.96[AMR][1000 genomes];0.95[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	esv2763951	chr6:120195400-120297444	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv886573	chr6:120284480-120409492	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:120279000-120288600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:120282800-120288400	Weak transcription	Placenta Amnion	Placenta Amnion

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