Variant report

Variant	rs1619266
Chromosome Location	chr10:38054930-38054931
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10827823	0.85[ASN][1000 genomes]
rs10827824	0.85[ASN][1000 genomes]
rs10827825	0.85[ASN][1000 genomes]
rs10827828	0.83[ASN][1000 genomes]
rs10827829	0.80[ASN][1000 genomes]
rs10827831	0.80[ASN][1000 genomes]
rs11011346	0.82[EUR][1000 genomes]
rs11011354	0.85[ASN][1000 genomes]
rs11011355	0.85[ASN][1000 genomes]
rs11011363	0.83[ASN][1000 genomes]
rs11011366	0.83[ASN][1000 genomes]
rs11011370	0.83[ASN][1000 genomes]
rs11011372	0.83[ASN][1000 genomes]
rs11492508	0.83[ASN][1000 genomes]
rs11511139	0.85[ASN][1000 genomes]
rs11511141	0.85[ASN][1000 genomes]
rs11516808	0.83[ASN][1000 genomes]
rs11523837	0.83[ASN][1000 genomes]
rs11595684	0.83[ASN][1000 genomes]
rs11597286	0.80[ASN][1000 genomes]
rs11599689	0.88[ASN][1000 genomes]
rs1208645	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1208683	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1208695	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1208716	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1208770	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1208779	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1212108	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12267169	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12357391	0.82[ASN][1000 genomes]
rs12357418	0.82[ASN][1000 genomes]
rs12358094	0.85[ASN][1000 genomes]
rs12358108	0.85[ASN][1000 genomes]
rs12359608	0.83[ASN][1000 genomes]
rs12360411	0.85[ASN][1000 genomes]
rs12570939	0.85[ASN][1000 genomes]
rs12571820	0.85[ASN][1000 genomes]
rs12763390	0.83[ASN][1000 genomes]
rs12763409	0.83[ASN][1000 genomes]
rs12768391	0.83[ASN][1000 genomes]
rs12776092	0.83[EUR][1000 genomes]
rs12781703	0.85[ASN][1000 genomes]
rs12782327	0.83[ASN][1000 genomes]
rs12783272	0.86[EUR][1000 genomes]
rs12783666	0.85[ASN][1000 genomes]
rs12783722	0.85[ASN][1000 genomes]
rs1742235	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1779015	0.85[ASN][1000 genomes]
rs1779150	0.85[ASN][1000 genomes]
rs2076809	0.82[ASN][1000 genomes]
rs2753877	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2891586	0.80[ASN][1000 genomes]
rs34185758	0.83[EUR][1000 genomes]
rs34496143	0.82[ASN][1000 genomes]
rs35872666	0.80[ASN][1000 genomes]
rs35951606	0.83[ASN][1000 genomes]
rs3824584	0.83[ASN][1000 genomes]
rs3824585	0.80[ASN][1000 genomes]
rs61858625	0.82[ASN][1000 genomes]
rs61858626	0.82[ASN][1000 genomes]
rs61859667	0.85[ASN][1000 genomes]
rs61859679	0.88[ASN][1000 genomes]
rs72639533	0.82[ASN][1000 genomes]
rs7476802	0.82[EUR][1000 genomes]
rs9417261	0.80[ASN][1000 genomes]
rs9417263	0.80[ASN][1000 genomes]
rs9417265	0.80[ASN][1000 genomes]
rs9417267	0.83[ASN][1000 genomes]
rs9417268	0.80[ASN][1000 genomes]
rs9418288	0.80[ASN][1000 genomes]
rs9418289	0.80[ASN][1000 genomes]
rs9418291	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9418294	0.80[ASN][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:5 , 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	chr10:38049000-38056400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr10:38049000-38064800	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr10:38051800-38066000	Weak transcription	HepG2	liver

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