Variant report

Variant	rs9398963
Chromosome Location	chr6:131132903-131132904
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1008688	0.84[CEU][hapmap]
rs10457561	1.00[JPT][hapmap]
rs10457562	1.00[JPT][hapmap]
rs10457563	1.00[JPT][hapmap]
rs12176542	1.00[AFR][1000 genomes]
rs12197688	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12208586	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3777432	1.00[JPT][hapmap]
rs6942054	0.88[EUR][1000 genomes]
rs71551706	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9375773	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9375778	1.00[JPT][hapmap]
rs9385567	1.00[JPT][hapmap]
rs9388853	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9388854	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9388860	1.00[JPT][hapmap]
rs9398964	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9402283	0.88[EUR][1000 genomes]
rs9402295	1.00[JPT][hapmap]

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	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9398963	EPB41L2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131131200-131133600	Enhancers	HepG2	liver
2	chr6:131131800-131133400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:131132000-131138000	Weak transcription	Adipose Nuclei	Adipose
4	chr6:131132000-131141800	Weak transcription	Brain Anterior Caudate	brain
5	chr6:131132000-131159200	Weak transcription	HSMM	muscle
6	chr6:131132000-131173800	Weak transcription	HSMMtube	muscle

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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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