Variant report

Variant	esv3465725
Chromosome Location	chr4:93579815-93580380
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	chr4:93577929..93580454-chr4:93584774..93587320,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560751239	chr4:93579815-93579816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369145645	chr4:93579842-93579843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370017984	chr4:93579852-93579853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs62309215	chr4:93579865-93579866	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs143990922	chr4:93579868-93579869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185889585	chr4:93579902-93579903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116032413	chr4:93579918-93579919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190858799	chr4:93579926-93579927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367855535	chr4:93579931-93579932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200140109	chr4:93579941-93579942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62309216	chr4:93579942-93579943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141599775	chr4:93579943-93579944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs70942921	chr4:93579944-93579945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201480396	chr4:93579945-93579946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200074870	chr4:93579946-93579947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201222766	chr4:93579948-93579949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201581753	chr4:93579962-93579963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199797676	chr4:93579964-93579965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs62309218	chr4:93579971-93579972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183257675	chr4:93579983-93579984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146412622	chr4:93579987-93579988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568326218	chr4:93580085-93580086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537473733	chr4:93580089-93580090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9999906	chr4:93580098-93580099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187823697	chr4:93580216-93580217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34738616	chr4:93580220-93580221	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs191145275	chr4:93580226-93580227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556860797	chr4:93580242-93580243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558836654	chr4:93580247-93580248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201249940	chr4:93580271-93580272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139983013	chr4:93580274-93580275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bipolar disorder	19114987	CNVD
Autism	20841430	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:93579600-93580600	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr4:93579800-93590600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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