Variant report

Variant	rs11602033
Chromosome Location	chr11:107251712-107251713
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 124 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs1046094	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs1046095	1.00[JPT][hapmap]
rs10502087	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10749896	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs10749901	0.81[ASN][1000 genomes]
rs10749902	0.84[EUR][1000 genomes]
rs10789598	0.80[ASN][1000 genomes]
rs10789604	0.81[ASN][1000 genomes]
rs10789605	0.82[ASN][1000 genomes]
rs10789606	0.82[ASN][1000 genomes]
rs10789607	0.80[ASN][1000 genomes]
rs10789608	0.80[ASN][1000 genomes]
rs10789611	0.81[ASN][1000 genomes]
rs10789612	0.81[ASN][1000 genomes]
rs10789613	0.81[ASN][1000 genomes]
rs10789615	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10789616	0.86[CEU][hapmap];0.92[JPT][hapmap];0.81[ASN][1000 genomes]
rs10789617	1.00[JPT][hapmap]
rs10789618	1.00[JPT][hapmap]
rs10789620	0.86[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10789621	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10890695	0.82[ASN][1000 genomes]
rs10890696	0.80[ASN][1000 genomes]
rs10890697	0.80[ASN][1000 genomes]
rs10890699	0.80[ASN][1000 genomes]
rs10890701	0.80[ASN][1000 genomes]
rs10890704	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10890705	0.81[ASN][1000 genomes]
rs10890707	0.81[ASN][1000 genomes]
rs10890708	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10890709	0.81[ASN][1000 genomes]
rs10890712	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10890715	0.81[ASN][1000 genomes]
rs10890716	0.81[ASN][1000 genomes]
rs10890717	0.87[EUR][1000 genomes]
rs10890718	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10890719	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10890720	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10890721	0.91[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10890723	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11212138	0.82[ASN][1000 genomes]
rs11212141	0.80[ASN][1000 genomes]
rs11212142	0.80[ASN][1000 genomes]
rs11212143	0.80[ASN][1000 genomes]
rs11212153	0.80[ASN][1000 genomes]
rs11212156	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11212157	0.81[ASN][1000 genomes]
rs11212158	0.81[ASN][1000 genomes]
rs11212159	0.81[ASN][1000 genomes]
rs11212160	0.81[ASN][1000 genomes]
rs11212162	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11212163	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11212164	0.81[ASN][1000 genomes]
rs11212166	0.86[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11212173	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11212175	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11212177	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11212179	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11212180	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11212181	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11212182	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11212197	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11212206	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11212207	0.80[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11607304	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12146472	0.81[ASN][1000 genomes]
rs12146473	0.81[ASN][1000 genomes]
rs12223855	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12270655	0.81[ASN][1000 genomes]
rs12285491	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12285607	0.80[ASN][1000 genomes]
rs12286915	0.86[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1490946	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1490947	0.89[EUR][1000 genomes]
rs17106875	0.85[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2046903	0.80[ASN][1000 genomes]
rs2161965	0.99[ASN][1000 genomes]
rs2356280	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3758911	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4343000	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4387327	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4576794	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55837508	0.81[ASN][1000 genomes]
rs56393657	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56753250	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs588921	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs590699	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs59525924	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs624584	0.90[EUR][1000 genomes]
rs6421541	1.00[YRI][hapmap]
rs655448	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6588964	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6588965	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs671493	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs687991	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7117615	0.91[ASN][1000 genomes]
rs7131522	0.80[ASN][1000 genomes]
rs72990438	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72990443	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7350479	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7358296	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7358308	0.86[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs999984	0.91[CEU][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs999985	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898364	chr11:106944975-107285636	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv898365	chr11:106944975-107430300	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv898366	chr11:106944975-107433835	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv898367	chr11:106944975-107443420	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv898369	chr11:106958304-107443420	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv898370	chr11:107027991-107430300	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv898372	chr11:107049968-107433835	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1038368	chr11:107116577-107664181	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription 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	17 gene(s)	inside rSNPs	diseases
9	nsv541163	chr11:107116577-107664181	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	nsv898373	chr11:107124903-107433835	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv832261	chr11:107145901-107321562	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv898374	chr11:107156880-107263130	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	esv2756363	chr11:107189790-107376790	ZNF genes & repeats Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
14	nsv475	chr11:107211800-107255722	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	nsv75	chr11:107219624-107251780	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
16	nsv508655	chr11:107222641-107257485	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
17	esv1805814	chr11:107238644-107252350	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
18	esv1812015	chr11:107239106-107257165	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
19	nsv556337	chr11:107239806-107255940	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
20	nsv556376	chr11:107250851-107486598	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107195000-107299200	Weak transcription	Colon Smooth Muscle	Colon
2	chr11:107219800-107256400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr11:107221800-107258400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr11:107223000-107253000	Weak transcription	Liver	Liver
5	chr11:107223000-107253600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr11:107223000-107256400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr11:107223000-107260600	Weak transcription	Brain Anterior Caudate	brain
8	chr11:107223000-107260600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr11:107224000-107258400	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr11:107224600-107253400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr11:107225800-107256400	Weak transcription	Adipose Nuclei	Adipose
12	chr11:107230000-107253400	Weak transcription	Lung	lung
13	chr11:107230200-107261400	Weak transcription	Ovary	ovary
14	chr11:107232400-107257800	Weak transcription	Primary B cells from peripheral blood	blood
15	chr11:107239400-107253400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr11:107240600-107261800	Weak transcription	Fetal Lung	lung
17	chr11:107241000-107253000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:107241600-107261200	Weak transcription	Fetal Kidney	kidney
19	chr11:107241600-107327800	Weak transcription	HSMMtube	muscle
20	chr11:107243400-107254600	Weak transcription	NHEK	skin
21	chr11:107243800-107267600	Weak transcription	Gastric	stomach
22	chr11:107244200-107254400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr11:107245200-107256400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr11:107247200-107254600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr11:107247600-107259400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:107248000-107260000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr11:107248600-107255800	Weak transcription	HepG2	liver
28	chr11:107248600-107260800	Weak transcription	Brain Hippocampus Middle	brain
29	chr11:107248600-107261400	Weak transcription	Thymus	Thymus
30	chr11:107248800-107252800	Weak transcription	Primary B cells from cord blood	blood
31	chr11:107249000-107261000	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr11:107249000-107267600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr11:107249200-107260000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr11:107249400-107260600	Weak transcription	Primary hematopoietic stem cells	blood
35	chr11:107249800-107253000	Weak transcription	Primary T cells from cord blood	blood
36	chr11:107249800-107256400	Weak transcription	NHDF-Ad	bronchial
37	chr11:107249800-107259600	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr11:107250200-107256600	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr11:107250200-107260000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr11:107250200-107261800	Weak transcription	Psoas Muscle	Psoas
41	chr11:107250400-107252800	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr11:107250400-107253400	Weak transcription	Aorta	Aorta
43	chr11:107250400-107253600	Weak transcription	Fetal Intestine Small	intestine
44	chr11:107250400-107253600	Weak transcription	Dnd41	blood
45	chr11:107250400-107256200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr11:107250400-107257800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr11:107250800-107256400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr11:107250800-107258400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr11:107251000-107260000	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr11:107251400-107253400	Weak transcription	Left Ventricle	heart

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