Variant report

Variant	rs11155661
Chromosome Location	chr6:101229025-101229026
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs1039033	0.82[EUR][1000 genomes]
rs1099916	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11155673	0.81[ASN][1000 genomes]
rs11755579	0.88[CHB][hapmap]
rs11756783	0.97[ASN][1000 genomes]
rs11758174	0.88[CHB][hapmap];1.00[YRI][hapmap]
rs11758891	0.99[ASN][1000 genomes]
rs11759127	1.00[YRI][hapmap]
rs11967951	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12174806	0.81[ASN][1000 genomes]
rs12175456	0.81[ASN][1000 genomes]
rs12202621	0.81[ASN][1000 genomes]
rs12215909	0.81[EUR][1000 genomes]
rs12525128	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12525818	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12526352	0.97[ASN][1000 genomes]
rs12528607	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13201267	0.96[ASN][1000 genomes]
rs13217436	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1414734	0.80[EUR][1000 genomes]
rs17190683	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs17794439	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1813223	0.88[CHB][hapmap];1.00[YRI][hapmap]
rs2004276	1.00[YRI][hapmap]
rs2050549	0.81[ASN][1000 genomes]
rs2101814	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2134044	0.95[ASN][1000 genomes]
rs2398247	1.00[YRI][hapmap]
rs3811078	0.82[JPT][hapmap]
rs3818233	0.95[ASN][1000 genomes]
rs4463266	0.81[ASN][1000 genomes]
rs4839789	0.81[ASN][1000 genomes]
rs4840153	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4840154	0.81[ASN][1000 genomes]
rs4840157	0.81[CEU][hapmap];0.94[CHB][hapmap];0.82[JPT][hapmap]
rs62422070	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6570969	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6570970	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6905113	0.81[ASN][1000 genomes]
rs6917195	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6919283	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6925316	0.81[ASN][1000 genomes]
rs6927598	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6937520	0.81[EUR][1000 genomes]
rs705586	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs723742	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs723743	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7746961	0.81[ASN][1000 genomes]
rs7759463	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9322173	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9322181	0.81[ASN][1000 genomes]
rs9322182	0.81[ASN][1000 genomes]
rs9322183	0.81[ASN][1000 genomes]
rs9322212	0.82[JPT][hapmap]
rs9322216	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9373571	0.96[ASN][1000 genomes]
rs9373574	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9373590	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9377085	0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs9377193	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9377214	0.81[ASN][1000 genomes]
rs9377232	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9377234	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9377235	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9377241	0.87[CHB][hapmap]
rs9386250	0.81[ASN][1000 genomes]
rs9390502	0.93[ASN][1000 genomes]
rs9390626	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9390675	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9390679	0.81[ASN][1000 genomes]
rs9390681	0.81[ASN][1000 genomes]
rs9390682	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9390693	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9390695	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9390698	0.81[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap]
rs9399641	0.97[ASN][1000 genomes]
rs9399656	0.98[ASN][1000 genomes]
rs9399685	0.81[ASN][1000 genomes]
rs9399688	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9403962	0.98[ASN][1000 genomes]
rs9404022	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9404031	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9404033	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9404045	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9404049	0.81[ASN][1000 genomes]
rs964223	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs979122	0.94[CHB][hapmap];0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949535	chr6:100740293-101469052	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv886445	chr6:101004751-101240763	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv886456	chr6:101049108-101277926	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1020692	chr6:101136992-101426071	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS 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	8 gene(s)	inside rSNPs	diseases
5	nsv604275	chr6:101158950-101277926	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv886457	chr6:101158950-101487473	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv1016353	chr6:101172705-101304041	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv1020400	chr6:101172705-101981665	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv538390	chr6:101172705-101981665	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
10	nsv1024526	chr6:101192726-101241291	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1019213	chr6:101225650-101623140	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer 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	8 gene(s)	inside rSNPs	diseases
12	nsv538391	chr6:101225650-101623140	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101184400-101304600	Weak transcription	Hela-S3	cervix
2	chr6:101191400-101277000	Weak transcription	Esophagus	oesophagus
3	chr6:101211800-101231800	Weak transcription	Pancreas	Pancrea
4	chr6:101212000-101246400	Weak transcription	Psoas Muscle	Psoas
5	chr6:101212000-101276200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:101212000-101281400	Weak transcription	Aorta	Aorta
7	chr6:101213200-101242800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:101213400-101244000	Weak transcription	HSMMtube	muscle
9	chr6:101213600-101241600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr6:101213600-101256000	Weak transcription	Ovary	ovary
11	chr6:101213600-101281600	Weak transcription	Gastric	stomach
12	chr6:101213800-101237000	Weak transcription	Primary T cells from cord blood	blood
13	chr6:101213800-101250800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr6:101213800-101254200	Weak transcription	Fetal Thymus	thymus
15	chr6:101214600-101236400	Weak transcription	GM12878-XiMat	blood
16	chr6:101214800-101281600	Weak transcription	Left Ventricle	heart
17	chr6:101215200-101237000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr6:101215200-101237400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:101215200-101242200	Weak transcription	Primary B cells from peripheral blood	blood
20	chr6:101215200-101244000	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr6:101215200-101244000	Weak transcription	Liver	Liver
22	chr6:101215200-101244000	Weak transcription	Placenta	Placenta
23	chr6:101215200-101247000	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr6:101215200-101252600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr6:101215200-101256200	Weak transcription	Osteobl	bone
26	chr6:101215200-101263000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr6:101215200-101311400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:101215400-101234800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr6:101215400-101239800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr6:101215400-101242000	Weak transcription	Primary B cells from cord blood	blood
31	chr6:101215400-101243400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:101215400-101243400	Weak transcription	NHDF-Ad	bronchial
33	chr6:101215400-101243600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr6:101215400-101243600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr6:101215400-101244000	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr6:101215400-101244000	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr6:101215400-101258600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr6:101215600-101242400	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr6:101215600-101242600	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr6:101216200-101241800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr6:101217400-101231200	Weak transcription	Dnd41	blood
42	chr6:101223000-101244200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr6:101223000-101256800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:101223400-101242200	Weak transcription	NH-A	brain
45	chr6:101223400-101243600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:101225600-101233400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr6:101226000-101243600	Weak transcription	HSMM	muscle
48	chr6:101226000-101281400	Weak transcription	HUVEC	blood vessel
49	chr6:101226600-101237800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:101228800-101236400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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