Variant report

Variant	rs12357391
Chromosome Location	chr10:37978474-37978475
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:37976754..37978580-chr10:37994431..37996961,2	K562	blood:

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10827823	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10827824	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10827825	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10827828	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10827829	0.91[ASN][1000 genomes]
rs10827831	0.91[ASN][1000 genomes]
rs11011284	0.85[ASN][1000 genomes]
rs11011287	0.85[ASN][1000 genomes]
rs11011326	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11011328	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11011330	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11011331	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11011334	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11011354	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11011355	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11011363	0.95[ASN][1000 genomes]
rs11011366	0.95[ASN][1000 genomes]
rs11011370	0.95[ASN][1000 genomes]
rs11011372	0.95[ASN][1000 genomes]
rs11011378	0.85[EUR][1000 genomes]
rs11492508	0.95[ASN][1000 genomes]
rs11511139	0.97[ASN][1000 genomes]
rs11511141	0.97[ASN][1000 genomes]
rs11516808	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11523837	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11595684	0.95[ASN][1000 genomes]
rs11597286	0.91[ASN][1000 genomes]
rs11599689	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1208645	0.91[ASN][1000 genomes]
rs1208683	0.93[ASN][1000 genomes]
rs1208695	0.95[ASN][1000 genomes]
rs1208716	0.95[ASN][1000 genomes]
rs1208770	0.97[ASN][1000 genomes]
rs1208779	0.95[ASN][1000 genomes]
rs1209425	0.84[ASN][1000 genomes]
rs1212108	0.95[ASN][1000 genomes]
rs12267169	0.93[ASN][1000 genomes]
rs12355532	0.82[ASN][1000 genomes]
rs12357418	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12358094	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12358108	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12359608	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12360411	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12570939	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12571820	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12763390	0.95[ASN][1000 genomes]
rs12763409	0.95[ASN][1000 genomes]
rs12768391	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12781703	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12782327	0.95[ASN][1000 genomes]
rs12783666	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12783722	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1619266	0.82[ASN][1000 genomes]
rs1742235	0.97[ASN][1000 genomes]
rs1779015	0.97[ASN][1000 genomes]
rs1779150	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2076809	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753877	0.97[ASN][1000 genomes]
rs2891586	0.91[ASN][1000 genomes]
rs34496143	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35215319	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35872666	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35951606	0.95[ASN][1000 genomes]
rs35954589	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3824584	0.95[ASN][1000 genomes]
rs3824585	0.91[ASN][1000 genomes]
rs61857913	0.85[ASN][1000 genomes]
rs61858625	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61858626	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61859667	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61859679	0.93[ASN][1000 genomes]
rs72639533	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9417261	0.91[ASN][1000 genomes]
rs9417262	0.81[ASN][1000 genomes]
rs9417263	0.91[ASN][1000 genomes]
rs9417264	0.88[ASN][1000 genomes]
rs9417265	0.91[ASN][1000 genomes]
rs9417267	0.88[ASN][1000 genomes]
rs9417268	0.91[ASN][1000 genomes]
rs9418288	0.91[ASN][1000 genomes]
rs9418289	0.91[ASN][1000 genomes]
rs9418291	0.91[ASN][1000 genomes]
rs9418294	0.91[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	nsv6443	chr10:37949704-37995270	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	esv1794823	chr10:37961177-38002067	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:37977800-37979200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell

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