Variant report

Variant	rs6134882
Chromosome Location	chr20:13468797-13468798
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	chr20:13467756..13469452-chr20:13473202..13474865,2	MCF-7	breast:

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs11698396	0.91[CHB][hapmap];0.82[JPT][hapmap];0.80[ASN][1000 genomes]
rs11698691	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12329562	0.89[CHB][hapmap];0.93[JPT][hapmap];0.96[ASN][1000 genomes]
rs13041649	0.80[ASN][1000 genomes]
rs1973948	0.85[CHB][hapmap];0.93[JPT][hapmap]
rs2073323	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2327789	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28444692	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2876356	0.95[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3789343	0.90[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3789344	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3789345	0.95[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3789350	0.95[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4411781	0.95[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6033712	0.81[YRI][hapmap]
rs6033720	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6033723	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6033727	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6033731	0.95[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6033733	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6033735	0.95[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6033736	0.91[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6033737	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6033741	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6033745	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6033755	0.91[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6042156	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6042167	0.91[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6042174	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6042176	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6042179	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6042181	0.95[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6042183	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6042184	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6042186	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6042212	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6042222	0.92[CHB][hapmap];0.93[JPT][hapmap]
rs6105115	0.95[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6105116	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6109906	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6109908	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6109913	0.95[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6109915	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6131478	0.95[ASN][1000 genomes]
rs6131480	0.92[CHB][hapmap];0.92[JPT][hapmap];0.95[ASN][1000 genomes]
rs6131481	0.95[ASN][1000 genomes]
rs6131482	0.91[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6134872	0.86[ASN][1000 genomes]
rs6134883	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6134885	0.91[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6134890	0.95[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6134892	0.92[CHB][hapmap];0.93[JPT][hapmap];0.95[ASN][1000 genomes]
rs6134893	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6134894	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6134896	0.91[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6134897	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6134899	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6134904	0.90[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6134907	0.92[CHB][hapmap];0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs6134908	0.85[ASN][1000 genomes]
rs6134909	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6134911	0.80[ASN][1000 genomes]
rs6134913	0.90[CEU][hapmap];0.92[CHB][hapmap];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6134914	0.93[CHB][hapmap];0.93[JPT][hapmap];0.80[ASN][1000 genomes]
rs6134915	0.80[ASN][1000 genomes]
rs6134918	0.93[CHB][hapmap];0.93[JPT][hapmap]
rs73080067	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73080080	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73086022	0.80[ASN][1000 genomes]
rs73086039	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8115098	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8123095	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs8126063	0.93[CHB][hapmap];0.93[JPT][hapmap];0.95[ASN][1000 genomes]
rs8184309	0.93[CHB][hapmap];0.92[JPT][hapmap];0.80[ASN][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	nsv1062049	chr20:13347580-13477455	Enhancers ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv544186	chr20:13347580-13477455	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1061303	chr20:13395546-13810990	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv585435	chr20:13410638-13582476	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv916202	chr20:13421724-14043615	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv1059817	chr20:13422602-13807968	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv458871	chr20:13447896-13573415	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv585436	chr20:13447896-13573415	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv1066810	chr20:13451869-14432454	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:13395600-13477800	Weak transcription	Gastric	stomach
2	chr20:13442600-13471600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr20:13454400-13471200	Weak transcription	Small Intestine	intestine
4	chr20:13457000-13471400	Weak transcription	Hela-S3	cervix
5	chr20:13458000-13470600	Weak transcription	Colon Smooth Muscle	Colon
6	chr20:13458000-13471600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr20:13458600-13472600	Weak transcription	Psoas Muscle	Psoas
8	chr20:13459400-13472000	Weak transcription	HSMMtube	muscle
9	chr20:13459600-13469800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr20:13459600-13472600	Weak transcription	NH-A	brain
11	chr20:13460200-13471600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr20:13460600-13469800	Weak transcription	Fetal Brain Female	brain
13	chr20:13460600-13472600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr20:13460800-13472000	Weak transcription	Brain Hippocampus Middle	brain
15	chr20:13460800-13472000	Weak transcription	NHEK	skin
16	chr20:13461400-13472000	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr20:13461800-13472000	Weak transcription	NHDF-Ad	bronchial
18	chr20:13462200-13471800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr20:13462200-13477800	Weak transcription	Thymus	Thymus
20	chr20:13463400-13471400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr20:13463400-13480200	Weak transcription	Brain Angular Gyrus	brain
22	chr20:13463600-13471600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr20:13463800-13471400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr20:13463800-13472000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr20:13463800-13481200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr20:13463800-13505400	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr20:13464000-13469400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr20:13464000-13469600	Weak transcription	Fetal Intestine Large	intestine
29	chr20:13464000-13469800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr20:13464000-13471600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr20:13464000-13472000	Weak transcription	Adipose Nuclei	Adipose
32	chr20:13464000-13472400	Weak transcription	A549	lung
33	chr20:13464000-13473800	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr20:13464000-13473800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr20:13464000-13474800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr20:13464000-13475200	Weak transcription	Fetal Kidney	kidney
37	chr20:13464000-13479000	Weak transcription	Duodenum Mucosa	Duodenum
38	chr20:13464000-13493800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr20:13464200-13469400	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr20:13464200-13471000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr20:13464200-13471400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr20:13464200-13471800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr20:13464200-13472000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr20:13464200-13472000	Weak transcription	HMEC	breast
45	chr20:13464200-13472600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr20:13464200-13472600	Weak transcription	Left Ventricle	heart
47	chr20:13464200-13472800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr20:13464200-13473000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr20:13464200-13475800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr20:13464200-13477800	Weak transcription	Primary hematopoietic stem cells	blood

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