Variant report

Variant	nsv604537
Chromosome Location	chr6:114224070-114224975
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:114224954-114225056	GM12878	blood:	n/a	n/a
2	REST	chr6:114224852-114225121	K562	blood:	n/a	chr6:114224979-114224992 chr6:114224983-114224992
3	REST	chr6:114224790-114225474	PFSK-1	brain:	n/a	chr6:114224979-114224992 chr6:114224983-114224992
4	REST	chr6:114224907-114225127	SK-N-SH	brain:	n/a	chr6:114224979-114224992 chr6:114224983-114224992
5	REST	chr6:114224710-114225535	PFSK-1	brain:	n/a	chr6:114224979-114224992 chr6:114224983-114224992
6	SIN3AK20	chr6:114224922-114225393	PFSK-1	brain:	n/a	n/a
7	TAF1	chr6:114224940-114225435	PFSK-1	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:114218743..114220678-chr6:114223116..114225137,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000175967	TF binding region

Extended variants
information (count: 30 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188434499	chr6:114224118-114224119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564775665	chr6:114224121-114224122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551049693	chr6:114224135-114224136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201190752	chr6:114224232-114224233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113927728	chr6:114224234-114224235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559851698	chr6:114224235-114224236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560092436	chr6:114224239-114224240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527529760	chr6:114224254-114224255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs397822658	chr6:114224256-114224257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574237300	chr6:114224282-114224283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191341272	chr6:114224295-114224296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532633215	chr6:114224337-114224338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534994625	chr6:114224383-114224384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567916401	chr6:114224400-114224401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377708661	chr6:114224488-114224489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs118159370	chr6:114224543-114224544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73551249	chr6:114224544-114224545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371774158	chr6:114224596-114224597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs151014687	chr6:114224604-114224605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6917232	chr6:114224631-114224632	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs566199539	chr6:114224647-114224648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571928554	chr6:114224767-114224768	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs183726421	chr6:114224778-114224779	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs554675576	chr6:114224794-114224795	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs573829529	chr6:114224820-114224821	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs578251619	chr6:114224910-114224911	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs140869163	chr6:114224916-114224917	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs59295167	chr6:114224922-114224923	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs539340709	chr6:114224937-114224938	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs189162821	chr6:114224968-114224969	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114223000-114225200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr6:114223000-114225200	Weak transcription	HUVEC	blood vessel
3	chr6:114223200-114225600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:114223400-114225000	Weak transcription	NHDF-Ad	bronchial
5	chr6:114223400-114225200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr6:114223400-114225200	Weak transcription	Osteobl	bone
7	chr6:114223600-114225000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr6:114223600-114225000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr6:114223600-114225200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:114223600-114225200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr6:114223800-114225000	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr6:114223800-114225200	Weak transcription	Colon Smooth Muscle	Colon
13	chr6:114223800-114225200	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr6:114224000-114225000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:114224000-114225000	Weak transcription	Fetal Muscle Leg	muscle
16	chr6:114224000-114225000	Weak transcription	HepG2	liver
17	chr6:114224400-114225000	Weak transcription	Fetal Muscle Trunk	muscle
18	chr6:114224600-114226200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr6:114224800-114225000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr6:114224800-114225000	Enhancers	Stomach Smooth Muscle	stomach
21	chr6:114224800-114226000	Enhancers	Rectal Smooth Muscle	rectum
22	chr6:114224800-114226600	Enhancers	Fetal Stomach	stomach

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