Variant report

Variant	rs7314340
Chromosome Location	chr12:10717188-10717189
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10734838	0.83[AMR][1000 genomes]
rs10743910	0.84[AMR][1000 genomes]
rs10772317	0.86[AMR][1000 genomes]
rs10772318	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10772319	0.84[AMR][1000 genomes]
rs10772321	0.82[AMR][1000 genomes]
rs10772323	0.82[AMR][1000 genomes]
rs10772324	0.83[AMR][1000 genomes]
rs10772325	0.82[AMR][1000 genomes]
rs10772326	0.82[AMR][1000 genomes]
rs10772327	0.82[AMR][1000 genomes]
rs10845162	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10845164	0.86[AMR][1000 genomes]
rs10845166	0.86[AMR][1000 genomes]
rs10845167	0.87[AMR][1000 genomes]
rs10845168	0.89[AMR][1000 genomes]
rs10845174	0.81[AMR][1000 genomes]
rs11053869	0.82[AMR][1000 genomes]
rs11053870	0.82[AMR][1000 genomes]
rs2125092	0.82[AMR][1000 genomes]
rs2125095	0.84[AMR][1000 genomes]
rs2168750	0.82[AMR][1000 genomes]
rs2417747	0.81[AMR][1000 genomes]
rs3867478	0.82[AMR][1000 genomes]
rs3983545	0.82[AMR][1000 genomes]
rs3983546	0.82[AMR][1000 genomes]
rs3983547	0.82[AMR][1000 genomes]
rs4536307	0.83[AMR][1000 genomes]
rs4763550	0.86[AMR][1000 genomes]
rs4763551	0.86[AMR][1000 genomes]
rs4763553	0.86[AMR][1000 genomes]
rs4763556	0.81[AMR][1000 genomes]
rs4763558	0.93[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4763559	0.82[AMR][1000 genomes]
rs5005301	0.83[ASN][1000 genomes]
rs6488307	0.86[AMR][1000 genomes]
rs7134658	0.82[AMR][1000 genomes]
rs7134908	0.82[AMR][1000 genomes]
rs7137465	0.81[AMR][1000 genomes]
rs7306285	0.82[AMR][1000 genomes]
rs7306724	0.82[AMR][1000 genomes]
rs7311860	0.86[AMR][1000 genomes]
rs7315514	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7955358	0.90[AMR][1000 genomes]
rs7955359	0.90[AMR][1000 genomes]
rs7964203	0.83[AMR][1000 genomes]
rs7965052	0.81[AMR][1000 genomes]
rs7978788	0.92[AMR][1000 genomes]
rs7979402	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7980411	0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898766	chr12:10537269-10722585	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv557459	chr12:10560591-10729821	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv898772	chr12:10622047-10722585	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv557479	chr12:10644663-10729821	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv898773	chr12:10660850-10722585	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv898774	chr12:10666025-10722585	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv898775	chr12:10668694-10735786	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv1039120	chr12:10675930-10755446	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	nsv832329	chr12:10677094-10845946	Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 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	chr12:10710800-10724800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:10714000-10733200	Weak transcription	Primary T cells from cord blood	blood
3	chr12:10714600-10718400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:10716000-10717800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr12:10716800-10723800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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