Variant report

Variant	rs634343
Chromosome Location	chr11:86887886-86887887
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs12576009	0.83[CHB][hapmap]
rs17212655	0.94[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2451060	0.94[CEU][hapmap]
rs301573	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs301577	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs301578	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs301581	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs301585	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs301587	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs301588	0.94[CEU][hapmap];0.90[JPT][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs301590	0.94[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs301591	0.95[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs471471	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs473364	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs476943	1.00[CEU][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs481278	0.81[CHB][hapmap]
rs492605	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs496834	1.00[CEU][hapmap];0.83[CHB][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs500109	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs502144	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs503939	1.00[CEU][hapmap];0.84[CHB][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs505429	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs516120	0.80[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs521252	0.84[CHB][hapmap]
rs529564	1.00[CEU][hapmap];0.83[CHB][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs533931	0.82[ASN][1000 genomes]
rs552253	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs556160	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs575992	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs576528	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs581174	1.00[CEU][hapmap];0.83[CHB][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs596912	0.86[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.84[ASN][1000 genomes]
rs604960	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs605313	1.00[CEU][hapmap];0.83[CHB][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs611538	0.91[CHB][hapmap];0.94[JPT][hapmap];0.88[YRI][hapmap];0.82[ASN][1000 genomes]
rs613715	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs619565	0.94[CEU][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs622517	0.80[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs622921	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs633211	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs637418	1.00[CEU][hapmap];0.85[CHB][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs651945	0.95[CEU][hapmap];0.81[JPT][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs672224	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs676384	0.83[CHB][hapmap]
rs7930231	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[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	nsv1037042	chr11:86586876-86978492	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv541119	chr11:86586876-86978492	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv898058	chr11:86754948-86889284	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv898059	chr11:86754948-86949369	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1043562	chr11:86755535-87547185	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv541120	chr11:86755535-87547185	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv1046288	chr11:86757573-87158571	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	nsv1045057	chr11:86794670-87033779	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 lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv541121	chr11:86794670-87033779	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv468777	chr11:86794856-86985581	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv555707	chr11:86794856-86985581	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv898060	chr11:86822077-86912633	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
13	nsv420	chr11:86845328-86890111	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv898061	chr11:86850483-86944982	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv468778	chr11:86850483-86974576	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv555708	chr11:86850483-86974576	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv898062	chr11:86864277-86902079	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv898063	chr11:86864277-86944982	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv898064	chr11:86864277-87013438	Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
20	esv2829956	chr11:86872504-87025059	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86867000-86888600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr11:86880600-86891800	Weak transcription	Aorta	Aorta
3	chr11:86880800-86892600	Weak transcription	Liver	Liver
4	chr11:86881000-86889000	Weak transcription	Fetal Intestine Small	intestine
5	chr11:86881800-86891000	Weak transcription	Thymus	Thymus
6	chr11:86882000-86928000	Weak transcription	Left Ventricle	heart
7	chr11:86883200-86889000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:86884200-86888000	Enhancers	Hela-S3	cervix
9	chr11:86884400-86891400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr11:86884600-86896600	Weak transcription	Fetal Kidney	kidney
11	chr11:86884600-86899200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr11:86884800-86901200	Weak transcription	K562	blood
13	chr11:86885000-86892000	Weak transcription	Brain Substantia Nigra	brain
14	chr11:86885000-86893200	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr11:86885000-86902200	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr11:86885200-86888000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr11:86885200-86888800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr11:86885200-86890800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:86885200-86891800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:86885400-86891600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr11:86885800-86889600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr11:86885800-86891800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr11:86886000-86888800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr11:86886200-86889600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr11:86886200-86894800	Weak transcription	Fetal Heart	heart
26	chr11:86886400-86896600	Weak transcription	Adipose Nuclei	Adipose
27	chr11:86886600-86891000	Weak transcription	HSMMtube	muscle
28	chr11:86886600-86891600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:86886800-86889000	Weak transcription	A549	lung
30	chr11:86886800-86890400	Weak transcription	HepG2	liver
31	chr11:86887200-86889000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr11:86887400-86889000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr11:86887400-86889600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr11:86887400-86891800	Weak transcription	Ovary	ovary
35	chr11:86887400-86899600	Weak transcription	NHDF-Ad	bronchial
36	chr11:86887600-86888800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr11:86887600-86889000	Weak transcription	Primary B cells from cord blood	blood
38	chr11:86887600-86890000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr11:86887600-86890200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:86887600-86893800	Weak transcription	NHLF	lung
41	chr11:86887600-86909400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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