Variant report

Variant	rs4936495
Chromosome Location	chr11:119568719-119568720
allele	C/T
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:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:119568589..119571498-chr11:119574354..119576763,2	MCF-7	breast:
2	chr11:119568263..119570489-chr11:119571275..119572812,2	K562	blood:
3	chr11:119568716..119570438-chr11:119574032..119575735,2	MCF-7	breast:
4	chr11:119551416..119553458-chr11:119566192..119569088,2	MCF-7	breast:
5	chr11:119553834..119555975-chr11:119568134..119570409,2	MCF-7	breast:
6	chr11:119567595..119569306-chr11:119571218..119572844,2	MCF-7	breast:
7	chr11:119568098..119571267-chr11:119595317..119602165,10	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000110400	Chromatin interaction
ENSG00000254854	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10790331	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10790332	0.82[AMR][1000 genomes]
rs10790335	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10892433	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10892434	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1110166	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11217414	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11217415	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11825206	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1467051	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1533051	0.81[AMR][1000 genomes]
rs2006949	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2015078	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2292293	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3902806	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3935405	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3935406	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4623916	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4936492	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4936493	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4936494	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4938708	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4938709	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4938710	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4938711	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6589769	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7110874	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7111290	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7124934	0.81[EUR][1000 genomes]
rs715849	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7924573	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7932832	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7933848	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7945395	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7945424	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7950059	0.90[EUR][1000 genomes]
rs885429	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs885430	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs906830	0.81[AMR][1000 genomes]

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	nsv898421	chr11:119499014-119631325	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv898422	chr11:119518006-119601779	Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv898423	chr11:119541332-119659753	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv468880	chr11:119564496-119588062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv556471	chr11:119564496-119588062	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119555800-119568800	Weak transcription	Left Ventricle	heart
2	chr11:119556000-119571600	Weak transcription	NHLF	lung
3	chr11:119559800-119570200	Enhancers	Fetal Thymus	thymus
4	chr11:119560400-119569600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr11:119561000-119580600	Weak transcription	Fetal Kidney	kidney
6	chr11:119561400-119568800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr11:119561800-119568800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr11:119561800-119577600	Enhancers	Brain Hippocampus Middle	brain
9	chr11:119562000-119578400	Enhancers	Duodenum Mucosa	Duodenum
10	chr11:119562400-119571000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:119562400-119571000	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr11:119563200-119578400	Genic enhancers	Fetal Intestine Small	intestine
13	chr11:119563600-119574000	Enhancers	Placenta	Placenta
14	chr11:119564200-119578400	Enhancers	Fetal Intestine Large	intestine
15	chr11:119564800-119571800	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr11:119565000-119569400	Weak transcription	Fetal Brain Female	brain
17	chr11:119565200-119582600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr11:119565400-119569400	Weak transcription	Brain Germinal Matrix	brain
19	chr11:119565400-119571400	Weak transcription	NH-A	brain
20	chr11:119565400-119571600	Weak transcription	Primary B cells from cord blood	blood
21	chr11:119565800-119569600	Weak transcription	Brain Anterior Caudate	brain
22	chr11:119565800-119569800	Weak transcription	Pancreas	Pancrea
23	chr11:119565800-119572400	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr11:119566400-119569400	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr11:119566400-119569600	Weak transcription	Brain Angular Gyrus	brain
26	chr11:119566400-119569800	Weak transcription	Liver	Liver
27	chr11:119566600-119569000	Weak transcription	Brain Substantia Nigra	brain
28	chr11:119567000-119572400	Enhancers	Stomach Mucosa	stomach
29	chr11:119567200-119568800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr11:119567200-119569000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr11:119567200-119569400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr11:119567200-119571800	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr11:119567200-119573200	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr11:119567200-119573600	Enhancers	Small Intestine	intestine
35	chr11:119567400-119569800	Weak transcription	Spleen	Spleen
36	chr11:119567400-119573400	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr11:119567400-119574400	Enhancers	Fetal Muscle Leg	muscle
38	chr11:119567400-119575000	Enhancers	Fetal Muscle Trunk	muscle
39	chr11:119567400-119576600	Weak transcription	Fetal Heart	heart
40	chr11:119567400-119579000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr11:119567600-119569600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:119567600-119572600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:119567800-119569000	Weak transcription	HepG2	liver
44	chr11:119567800-119569200	Weak transcription	Colonic Mucosa	Colon
45	chr11:119567800-119569800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr11:119567800-119569800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:119567800-119570000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr11:119567800-119570200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr11:119567800-119570400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:119567800-119572600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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