Variant report

Variant	rs11758794
Chromosome Location	chr6:161521680-161521681
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:161519466-161521806	K562	blood:	n/a	n/a
2	POLR2A	chr6:161521676-161521698	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:161521066..161521786-chr6:161794667..161795242,2	K562	blood:
2	chr6:161520982..161521822-chr6:161791879..161792471,2	MCF-7	breast:

Variant related genes	Relation type
MAP3K4	TF binding region

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1001421	1.00[CHB][hapmap]
rs1001422	1.00[CHB][hapmap]
rs1001756	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11751634	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs11751688	0.97[EUR][1000 genomes]
rs11751843	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11752188	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs11753446	0.83[EUR][1000 genomes]
rs11755042	0.87[EUR][1000 genomes]
rs11755244	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11757223	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs11757309	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11757882	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11759000	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11759408	1.00[CHB][hapmap]
rs11962121	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes]
rs12110827	1.00[CHB][hapmap]
rs1404269	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs1464781	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1534020	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs1562025	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes]
rs1807426	1.00[CHB][hapmap]
rs2009830	1.00[CHB][hapmap]
rs2314190	1.00[CHB][hapmap]
rs2314376	1.00[CHB][hapmap]
rs2314377	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3778218	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3778225	1.00[CHB][hapmap]
rs3798916	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3823057	1.00[CHB][hapmap];0.85[CHD][hapmap]
rs57922639	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58040353	0.87[EUR][1000 genomes]
rs59129068	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59318837	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6905734	1.00[CHB][hapmap]
rs6907956	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6922534	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6940321	1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs719474	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73784791	0.93[AFR][1000 genomes]
rs7738423	0.87[EUR][1000 genomes]
rs7754215	1.00[CHB][hapmap]
rs9365245	1.00[CHB][hapmap];0.85[CHD][hapmap]
rs9456635	1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9456636	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9458121	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9458135	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9458141	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030045	chr6:161359075-161562255	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv886817	chr6:161371621-161846654	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	esv3381361	chr6:161373617-161864101	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1023982	chr6:161382188-161549831	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv1030852	chr6:161477750-161589394	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161491000-161538400	Strong transcription	Primary B cells from peripheral blood	blood
2	chr6:161491600-161525400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
3	chr6:161491600-161528800	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr6:161491600-161529000	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr6:161491600-161539800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:161494400-161525600	Strong transcription	Dnd41	blood
7	chr6:161494400-161542400	Strong transcription	Duodenum Mucosa	Duodenum
8	chr6:161495200-161538000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr6:161496000-161539800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:161497800-161539600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:161498000-161541800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr6:161498600-161525600	Strong transcription	Primary T cells from cord blood	blood
13	chr6:161499000-161531800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr6:161500200-161540400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:161500400-161525600	Strong transcription	Adipose Nuclei	Adipose
16	chr6:161500600-161539800	Strong transcription	Rectal Mucosa Donor 29	rectum
17	chr6:161500600-161541800	Strong transcription	K562	blood
18	chr6:161500800-161538200	Strong transcription	Primary B cells from cord blood	blood
19	chr6:161502600-161531600	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr6:161503200-161532000	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr6:161504800-161531800	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr6:161505000-161524200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr6:161505000-161524400	Weak transcription	Psoas Muscle	Psoas
24	chr6:161505000-161528200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr6:161505800-161529800	Weak transcription	Fetal Brain Male	brain
26	chr6:161507000-161524000	Weak transcription	A549	lung
27	chr6:161509400-161528000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr6:161510600-161529000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:161510600-161531600	Weak transcription	Stomach Mucosa	stomach
30	chr6:161510800-161537400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr6:161512600-161528200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr6:161513200-161523400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr6:161513600-161523000	Weak transcription	Fetal Heart	heart
34	chr6:161514000-161544600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr6:161514200-161525400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr6:161514400-161524600	Strong transcription	HSMM	muscle
37	chr6:161514400-161539800	Strong transcription	Left Ventricle	heart
38	chr6:161514600-161541000	Strong transcription	Fetal Intestine Large	intestine
39	chr6:161515200-161526000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr6:161515400-161522600	Weak transcription	Brain Cingulate Gyrus	brain
41	chr6:161515400-161527600	Weak transcription	Brain Hippocampus Middle	brain
42	chr6:161515400-161528400	Weak transcription	Brain Angular Gyrus	brain
43	chr6:161517000-161539600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr6:161517200-161522600	Weak transcription	NHEK	skin
45	chr6:161517400-161523200	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr6:161517600-161523000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
47	chr6:161517600-161523400	Strong transcription	Thymus	Thymus
48	chr6:161517600-161525000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:161517600-161543000	Strong transcription	Skeletal Muscle Female	skeletal muscle
50	chr6:161517800-161525000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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