Variant report

Variant	esv3329173
Chromosome Location	chr1:176404521-176405019
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:176403551..176406184-chr1:176410216..176412303,2	K562	blood:

Extended variants
information (count: 17 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78770228	chr1:176404571-176404572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572783793	chr1:176404616-176404617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545212775	chr1:176404624-176404625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147210960	chr1:176404657-176404658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188942095	chr1:176404678-176404679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544826123	chr1:176404692-176404693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575340293	chr1:176404693-176404694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564547432	chr1:176404732-176404733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192213272	chr1:176404740-176404741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11590472	chr1:176404757-176404758	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs140612863	chr1:176404806-176404807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529318641	chr1:176404832-176404833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561142869	chr1:176404833-176404834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182883977	chr1:176404839-176404840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111309560	chr1:176404959-176404960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368370629	chr1:176404971-176404972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187340469	chr1:176404983-176404984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
early-passage human iPS cells	21368824	CNVD
Mental retardation	17847001	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:176403200-176404600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:176404600-176405600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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