Variant report

Variant	rs11498323
Chromosome Location	chr10:38057962-38057963
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10827830	0.85[AMR][1000 genomes]
rs11011356	0.85[AMR][1000 genomes]
rs11011357	0.85[AMR][1000 genomes]
rs11011358	0.85[AMR][1000 genomes]
rs11011375	0.85[AMR][1000 genomes]
rs11817696	0.85[AMR][1000 genomes]
rs11819551	0.85[AMR][1000 genomes]
rs12244864	0.85[AMR][1000 genomes]
rs12251570	0.85[AMR][1000 genomes]
rs12252091	0.85[AMR][1000 genomes]
rs12256181	0.85[AMR][1000 genomes]
rs12257632	0.85[AMR][1000 genomes]
rs12258024	0.85[AMR][1000 genomes]
rs12267923	0.85[AMR][1000 genomes]
rs12268435	0.85[AMR][1000 genomes]
rs12783599	0.85[AMR][1000 genomes]
rs34079297	0.85[AMR][1000 genomes]
rs34152840	0.85[AMR][1000 genomes]
rs34222428	0.85[AMR][1000 genomes]
rs34591573	0.85[AMR][1000 genomes]
rs34964888	0.85[AMR][1000 genomes]
rs35056062	0.85[AMR][1000 genomes]
rs35404142	0.85[AMR][1000 genomes]
rs35818588	0.85[AMR][1000 genomes]
rs36188980	1.00[AMR][1000 genomes]
rs71491203	0.85[AMR][1000 genomes]
rs71491212	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895030	chr10:37715737-38674609	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1045684	chr10:37765361-38426204	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv540564	chr10:37765361-38426204	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1040704	chr10:37940024-38451917	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	nsv975812	chr10:37990724-38084639	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv947608	chr10:38053801-38066317	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:38043600-38060800	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr10:38047000-38069400	Weak transcription	Ovary	ovary
3	chr10:38049000-38064800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr10:38051800-38066000	Weak transcription	HepG2	liver

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