Variant report

Variant	rs9321084
Chromosome Location	chr6:127728398-127728399
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs4285343	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4308584	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4487601	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4555941	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4897214	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6569488	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6912006	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6912196	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6912552	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6912750	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6914131	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6919082	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6919277	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6924274	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6934242	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6940199	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7762624	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7768435	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7769165	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9321081	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9321082	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9321083	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9321085	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9385422	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9385424	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9401958	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9401959	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9401960	0.81[AMR][1000 genomes]
rs9491775	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9491781	0.83[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3430461	chr6:127727308-127754317	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9321084	ECHDC1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:127720400-127729200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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