Variant report

Variant	rs17211787
Chromosome Location	chr11:86453783-86453784
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:86187402..86190173-chr11:86451965..86454595,2	MCF-7	breast:
2	chr11:86410588..86412313-chr11:86452715..86455271,2	K562	blood:
3	chr11:86452587..86455678-chr11:86498398..86501247,3	MCF-7	breast:
4	chr11:86450401..86454128-chr11:86509734..86516006,8	MCF-7	breast:
5	chr11:86451377..86454000-chr11:86469217..86471649,2	MCF-7	breast:
6	chr11:86429172..86438482-chr11:86450202..86456550,9	MCF-7	breast:
7	chr11:86382693..86386959-chr11:86452814..86456123,3	MCF-7	breast:
8	chr11:86422351..86424027-chr11:86451990..86454405,2	MCF-7	breast:
9	chr11:86412384..86414900-chr11:86452742..86454640,3	MCF-7	breast:
10	chr11:86453173..86455061-chr11:86477105..86479906,2	MCF-7	breast:
11	chr11:86452259..86454963-chr11:86491551..86494314,2	MCF-7	breast:
12	chr11:86447300..86456471-chr11:86483287..86490697,27	MCF-7	breast:
13	chr11:86445705..86457398-chr11:86504607..86518485,46	MCF-7	breast:
14	chr11:86445788..86450763-chr11:86452280..86455324,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000254731	Chromatin interaction
ENSG00000150687	Chromatin interaction
ENSG00000151376	Chromatin interaction
ENSG00000255250	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12420039	0.93[MEX][hapmap]
rs12576018	0.92[AMR][1000 genomes]
rs17819002	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17819068	0.88[AMR][1000 genomes]
rs17819187	0.93[MEX][hapmap]
rs1939111	0.93[MEX][hapmap]
rs1939113	0.82[CEU][hapmap]
rs2433431	0.86[MEX][hapmap]
rs2433432	0.86[MEX][hapmap]
rs2433433	0.86[MEX][hapmap]
rs2433434	0.86[MEX][hapmap]
rs2433439	0.93[MEX][hapmap]
rs2513003	0.86[MEX][hapmap]
rs3809048	1.00[MEX][hapmap]
rs4075249	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4128368	0.93[MEX][hapmap]
rs4269941	0.93[MEX][hapmap]
rs4304806	0.93[MEX][hapmap]
rs4423210	0.92[MEX][hapmap]
rs58823830	0.92[AMR][1000 genomes]
rs60023003	0.88[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044081	chr11:86133641-86868560	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv541118	chr11:86133641-86868560	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv1055071	chr11:86301240-86465465	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv428263	chr11:86357990-86508480	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1049157	chr11:86409059-86504155	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv521505	chr11:86438115-86515072	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv468775	chr11:86453415-86480716	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
8	nsv555705	chr11:86453415-86480716	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86446000-86458000	Enhancers	HMEC	breast
2	chr11:86446400-86455200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr11:86446800-86455400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr11:86447400-86455200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr11:86447600-86454200	Enhancers	NHDF-Ad	bronchial
6	chr11:86447800-86453800	Enhancers	Ovary	ovary
7	chr11:86448200-86454000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:86448400-86454200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:86448400-86456000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:86449000-86455000	Enhancers	Stomach Mucosa	stomach
11	chr11:86449000-86455200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:86449200-86455000	Enhancers	HepG2	liver
13	chr11:86449400-86454400	Enhancers	K562	blood
14	chr11:86449600-86455600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr11:86449800-86455000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:86449800-86455200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr11:86450200-86455200	Enhancers	Stomach Smooth Muscle	stomach
18	chr11:86450200-86459800	Enhancers	Placenta Amnion	Placenta Amnion
19	chr11:86450400-86455000	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr11:86450600-86454800	Enhancers	Right Atrium	heart
21	chr11:86450600-86455200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:86450800-86454000	Enhancers	HSMMtube	muscle
23	chr11:86450800-86455000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr11:86450800-86455200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr11:86451000-86454000	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr11:86451000-86454800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr11:86451000-86455200	Enhancers	Placenta	Placenta
28	chr11:86451200-86454000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr11:86452200-86455000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr11:86452200-86458000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr11:86452400-86454200	Weak transcription	Small Intestine	intestine
32	chr11:86452400-86454200	Enhancers	Osteobl	bone
33	chr11:86452400-86454400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr11:86452400-86457600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr11:86452600-86454000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr11:86452600-86454200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:86452600-86454600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr11:86452600-86455200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr11:86452800-86454200	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr11:86452800-86454600	Enhancers	NH-A	brain
41	chr11:86452800-86455200	Enhancers	NHLF	lung
42	chr11:86453000-86453800	Enhancers	Right Ventricle	heart
43	chr11:86453000-86454400	Enhancers	Aorta	Aorta
44	chr11:86453000-86454400	Enhancers	Lung	lung
45	chr11:86453000-86454600	Enhancers	Esophagus	oesophagus
46	chr11:86453000-86454600	Enhancers	Gastric	stomach
47	chr11:86453000-86454600	Enhancers	Left Ventricle	heart
48	chr11:86453000-86454600	Enhancers	HUVEC	blood vessel
49	chr11:86453000-86455000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr11:86453000-86457600	Weak transcription	Fetal Heart	heart

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