Variant report

Variant	rs4436897
Chromosome Location	chr2:148868188-148868189
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:148859675..148863197-chr2:148868107..148869963,3	MCF-7	breast:

Extended variants
information (count: 114 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs1015096	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs10178849	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10199458	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10207309	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10460259	0.82[CHB][hapmap];0.86[CHD][hapmap];0.90[JPT][hapmap]
rs10497029	0.82[EUR][1000 genomes]
rs11886876	0.86[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11888152	0.81[CHB][hapmap];0.86[CHD][hapmap];0.86[JPT][hapmap]
rs11896010	0.87[ASN][1000 genomes]
rs11901963	0.86[JPT][hapmap]
rs11902430	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12053401	0.81[CHD][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs12105411	0.88[ASN][1000 genomes]
rs12463798	0.86[JPT][hapmap]
rs12469509	0.83[EUR][1000 genomes]
rs12470955	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12691772	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12691773	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12691774	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12691775	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12691776	0.83[EUR][1000 genomes]
rs12691777	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12691778	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12691779	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12989250	0.86[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs12992231	0.85[ASN][1000 genomes]
rs12992412	0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs12995413	0.83[ASN][1000 genomes]
rs12997165	0.86[ASN][1000 genomes]
rs13006721	0.83[EUR][1000 genomes]
rs13007770	0.83[ASN][1000 genomes]
rs13008838	0.85[ASN][1000 genomes]
rs13013887	0.92[CEU][hapmap];0.82[JPT][hapmap];0.81[EUR][1000 genomes]
rs13014936	0.84[ASN][1000 genomes]
rs13015552	0.83[EUR][1000 genomes]
rs13015655	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13021605	0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs13022962	0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs13026650	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs13027706	0.86[JPT][hapmap]
rs13028348	0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs13029714	0.83[EUR][1000 genomes]
rs13032303	0.83[EUR][1000 genomes]
rs13032810	0.86[ASN][1000 genomes]
rs13035475	0.85[ASN][1000 genomes]
rs1449959	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1531032	0.86[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap]
rs1598207	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs16828270	0.83[EUR][1000 genomes]
rs16828354	0.82[EUR][1000 genomes]
rs1823447	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1901014	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1975748	0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs2084578	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2122386	0.83[EUR][1000 genomes]
rs2168145	0.85[ASN][1000 genomes]
rs2303392	0.85[JPT][hapmap]
rs2307394	0.81[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap]
rs2382211	0.83[EUR][1000 genomes]
rs2890915	0.87[ASN][1000 genomes]
rs35283425	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3768687	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs3768689	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs4001	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4417662	0.87[ASN][1000 genomes]
rs4972321	0.86[ASN][1000 genomes]
rs4972322	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4972329	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4972332	0.83[EUR][1000 genomes]
rs6430281	0.89[ASN][1000 genomes]
rs6430282	0.84[ASN][1000 genomes]
rs6430285	0.85[ASN][1000 genomes]
rs6430286	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6430289	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6430292	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6430295	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6711686	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6714672	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6724719	0.89[ASN][1000 genomes]
rs6729804	0.81[ASN][1000 genomes]
rs6730641	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6732463	0.89[ASN][1000 genomes]
rs6746415	0.89[ASN][1000 genomes]
rs7425436	0.80[ASN][1000 genomes]
rs7560425	0.87[ASN][1000 genomes]
rs7568811	0.83[EUR][1000 genomes]
rs7569780	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7574180	0.89[CEU][hapmap];0.82[JPT][hapmap];0.83[EUR][1000 genomes]
rs7592576	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7595067	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7595286	0.83[EUR][1000 genomes]
rs7598361	0.82[JPT][hapmap]
rs7604592	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs897172	0.81[CHD][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs9789434	0.83[ASN][1000 genomes]
rs9789640	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916286	chr2:148438001-148977722	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv529388	chr2:148471340-148934846	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1002358	chr2:148703807-148942372	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1007683	chr2:148717347-148942372	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv535971	chr2:148717347-148942372	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv817366	chr2:148727068-148879681	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1000852	chr2:148730825-148934986	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv535972	chr2:148730825-148934986	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv916766	chr2:148743880-148955720	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv1001339	chr2:148755022-149020866	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv535977	chr2:148755022-149020866	Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
12	nsv1014570	chr2:148780080-148869729	Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv535978	chr2:148780080-148869729	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv869146	chr2:148787051-149060763	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv875276	chr2:148844369-148996824	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv1004431	chr2:148859099-149054114	Weak transcription Active TSS ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
17	nsv997674	chr2:148862630-148995570	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
18	nsv1007998	chr2:148866051-148995570	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148854800-148874000	Weak transcription	Primary B cells from cord blood	blood
2	chr2:148855800-148901000	Weak transcription	Fetal Intestine Small	intestine
3	chr2:148861200-148889000	Weak transcription	Aorta	Aorta
4	chr2:148862000-148869800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr2:148863000-148881600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:148864000-148881200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr2:148864600-148883200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr2:148864800-148880200	Weak transcription	Osteobl	bone
9	chr2:148865000-148880200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:148865200-148868600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr2:148866200-148876400	Weak transcription	Fetal Lung	lung
12	chr2:148866600-148881000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:148867600-148868200	Enhancers	Primary T cells from cord blood	blood
14	chr2:148867600-148868200	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr2:148867600-148868400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr2:148867600-148868600	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr2:148867600-148869000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr2:148867600-148869000	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr2:148867800-148869000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr2:148867800-148869000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr2:148867800-148869000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr2:148868000-148868200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr2:148868000-148868400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr2:148868000-148868400	Flanking Active TSS	GM12878-XiMat	blood
25	chr2:148868000-148869200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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