Variant report

Variant	rs7585313
Chromosome Location	chr2:111975203-111975204
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10178095	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10179596	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11123421	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11681574	1.00[ASN][1000 genomes]
rs13391770	1.00[ASN][1000 genomes]
rs13431174	1.00[ASN][1000 genomes]
rs2137168	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2175505	0.98[ASN][1000 genomes]
rs28638111	0.92[ASN][1000 genomes]
rs28766030	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28871990	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56693625	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61358692	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6716091	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6727313	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6747657	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6749633	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67816163	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72837858	1.00[ASN][1000 genomes]
rs72837863	1.00[ASN][1000 genomes]
rs72837865	1.00[ASN][1000 genomes]
rs7600458	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874838	chr2:111376870-112046226	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv834331	chr2:111812139-112004678	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	esv1803356	chr2:111899783-112662597	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv428402	chr2:111899783-112662597	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
5	esv1801950	chr2:111899783-112746937	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
6	esv2757825	chr2:111899783-112746937	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	esv2759083	chr2:111899783-112746937	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
8	nsv874843	chr2:111966947-112023328	Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111954800-112006800	Weak transcription	HUVEC	blood vessel
2	chr2:111967200-111976400	Weak transcription	NH-A	brain
3	chr2:111972000-111977000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr2:111972400-111984400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr2:111972800-111982800	Weak transcription	HepG2	liver
6	chr2:111973000-111977200	Weak transcription	A549	lung
7	chr2:111973000-111979600	Weak transcription	Adipose Nuclei	Adipose
8	chr2:111973200-111977600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr2:111974200-111975400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:111974400-111975600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr2:111974600-111976000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:111974800-111975400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
13	chr2:111974800-111975400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr2:111974800-111975400	Strong transcription	HSMMtube	muscle
15	chr2:111974800-111984800	Weak transcription	NHDF-Ad	bronchial
16	chr2:111975000-111976400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr2:111975000-111976800	Weak transcription	HSMM	muscle
18	chr2:111975000-111977000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr2:111975000-111978800	Weak transcription	Aorta	Aorta
20	chr2:111975000-111985600	Weak transcription	Esophagus	oesophagus
21	chr2:111975200-111975400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr2:111975200-111975400	Active TSS	Placenta Amnion	Placenta Amnion
23	chr2:111975200-111975800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:111975200-111976200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr2:111975200-111976600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr2:111975200-111976800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr2:111975200-111976800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr2:111975200-111977800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:111975200-111979400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:111975200-111979400	Weak transcription	Left Ventricle	heart
31	chr2:111975200-111979400	Weak transcription	Spleen	Spleen
32	chr2:111975200-111979600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:111975200-111979600	Weak transcription	Right Atrium	heart
34	chr2:111975200-111980200	Weak transcription	Right Ventricle	heart
35	chr2:111975200-112008200	Weak transcription	Pancreas	Pancrea

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