Variant report

Variant	rs6132620
Chromosome Location	chr20:23436654-23436655
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	chr20:23435629..23437264-chr20:23438674..23441153,2	MCF-7	breast:

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs1076776	0.81[ASN][1000 genomes]
rs12625160	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12625999	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12626013	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17830565	0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2073300	1.00[CEU][hapmap]
rs2207988	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2207989	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2236021	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2277765	0.81[ASN][1000 genomes]
rs28407103	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34449811	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34740966	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35810824	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs36165478	0.81[ASN][1000 genomes]
rs3746737	0.81[ASN][1000 genomes]
rs57021299	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs59283536	0.88[ASN][1000 genomes]
rs6036411	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6036422	0.88[ASN][1000 genomes]
rs6036423	1.00[CEU][hapmap];0.88[ASN][1000 genomes]
rs6036424	1.00[CEU][hapmap];0.88[ASN][1000 genomes]
rs6048803	1.00[CEU][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6048809	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6048810	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6048811	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6048813	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6048814	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6048820	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6048822	1.00[CEU][hapmap];0.84[AMR][1000 genomes]
rs6048824	0.88[ASN][1000 genomes]
rs6048825	0.88[ASN][1000 genomes]
rs6048826	0.88[ASN][1000 genomes]
rs6048833	0.88[ASN][1000 genomes]
rs6048834	0.88[ASN][1000 genomes]
rs6048835	0.88[ASN][1000 genomes]
rs6083135	1.00[CEU][hapmap]
rs6083136	0.84[AMR][1000 genomes]
rs6106655	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6106656	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6106667	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6106669	1.00[CEU][hapmap];0.88[ASN][1000 genomes]
rs61080017	0.88[ASN][1000 genomes]
rs6114094	1.00[CEU][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6114098	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6114100	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6114101	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6114126	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6114135	0.88[ASN][1000 genomes]
rs6114136	0.81[ASN][1000 genomes]
rs6114137	0.81[ASN][1000 genomes]
rs6114138	0.87[ASN][1000 genomes]
rs6114139	0.88[ASN][1000 genomes]
rs6114141	1.00[CEU][hapmap];0.88[ASN][1000 genomes]
rs6114142	1.00[CEU][hapmap];0.88[ASN][1000 genomes]
rs6114144	1.00[CEU][hapmap];0.88[ASN][1000 genomes]
rs6132621	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6132622	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6132623	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6132626	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6132628	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6132629	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6132630	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6132631	1.00[CEU][hapmap];0.88[ASN][1000 genomes]
rs6137951	0.83[ASN][1000 genomes]
rs6137957	1.00[CEU][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6137959	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6137960	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6137961	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6137962	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6137963	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6137964	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6137967	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6137971	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6137975	1.00[CEU][hapmap];0.88[ASN][1000 genomes]
rs6137976	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6137977	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6137980	0.83[EUR][1000 genomes]
rs6137982	0.83[EUR][1000 genomes]
rs6137983	0.83[EUR][1000 genomes]
rs6137984	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063655	chr20:23396649-23489730	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv912818	chr20:23406519-23567838	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv912819	chr20:23406519-23569400	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv912820	chr20:23406519-23578148	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv1065390	chr20:23412890-23569238	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv1065719	chr20:23415029-23565333	Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv544214	chr20:23415029-23565333	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
8	nsv470544	chr20:23424638-23569400	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
9	nsv585722	chr20:23424638-23569400	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
10	nsv458949	chr20:23426648-23569400	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
11	nsv585723	chr20:23426648-23569400	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
12	nsv979404	chr20:23429655-23455778	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	nsv1057992	chr20:23430887-23565333	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
14	nsv544215	chr20:23430887-23565333	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
15	esv3405547	chr20:23432652-23436950	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
16	nsv491876	chr20:23436633-24031374	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23417800-23441000	Weak transcription	Right Atrium	heart
2	chr20:23432600-23446000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr20:23433800-23437000	Weak transcription	Fetal Stomach	stomach
4	chr20:23434000-23440400	Enhancers	Fetal Thymus	thymus
5	chr20:23434800-23445200	Weak transcription	Esophagus	oesophagus
6	chr20:23435200-23439800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr20:23435600-23437400	Enhancers	Primary T cells fromperipheralblood	blood
8	chr20:23436000-23436800	Enhancers	Dnd41	blood
9	chr20:23436200-23436800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr20:23436200-23438000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr20:23436200-23438000	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr20:23436400-23437400	Enhancers	Thymus	Thymus
13	chr20:23436400-23438200	Enhancers	Primary T cells from cord blood	blood
14	chr20:23436400-23438600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr20:23436400-23441000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr20:23436600-23437000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
17	chr20:23436600-23437200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
18	chr20:23436600-23437400	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr20:23436600-23437400	Enhancers	Fetal Muscle Leg	muscle
20	chr20:23436600-23438000	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr20:23436600-23439400	Enhancers	Primary hematopoietic stem cells	blood

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