Variant report

Variant	esv1963217
Chromosome Location	chr6:114647056-114647515
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146344781	chr6:114647091-114647092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs113223876	chr6:114647105-114647106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs58800329	chr6:114647127-114647128	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs546010489	chr6:114647156-114647157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527964923	chr6:114647162-114647163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549729120	chr6:114647202-114647203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561517349	chr6:114647246-114647247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185566124	chr6:114647254-114647255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550246438	chr6:114647257-114647258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571609018	chr6:114647274-114647275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532063068	chr6:114647282-114647283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532484088	chr6:114647315-114647316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs796769	chr6:114647321-114647322	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs565764411	chr6:114647344-114647345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149990152	chr6:114647350-114647351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145390622	chr6:114647409-114647410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567448821	chr6:114647467-114647468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113945333	chr6:114647502-114647503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144780708	chr6:114647511-114647512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
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
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
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
Urothelial carcinoma	21177765	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Salivary gland tumor	18059337	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Acute myeloid leukemia	19651600	CNVD

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114637600-114649600	Weak transcription	Brain Substantia Nigra	brain
2	chr6:114637600-114652200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr6:114640400-114651000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr6:114643000-114649600	Weak transcription	Brain Hippocampus Middle	brain
5	chr6:114644000-114648000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:114644400-114651600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:114645200-114649800	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr6:114645400-114652400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr6:114646000-114648400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr6:114646000-114648400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:114646000-114648400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr6:114646200-114647800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr6:114646200-114649800	Weak transcription	Brain Angular Gyrus	brain
14	chr6:114646400-114647600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr6:114646400-114648000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:114646600-114648000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr6:114646600-114655400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr6:114647000-114651600	Enhancers	HUES6 Cell Line	embryonic stem cell

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