Variant report

Variant	esv2344651
Chromosome Location	chr9:15602390-15602760
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79293668	chr9:15602412-15602413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189231757	chr9:15602415-15602416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549453485	chr9:15602453-15602454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193095596	chr9:15602469-15602470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577104556	chr9:15602475-15602476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183700084	chr9:15602488-15602489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2663298	chr9:15602519-15602520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553232754	chr9:15602520-15602521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574708235	chr9:15602560-15602561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187225932	chr9:15602569-15602570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563774664	chr9:15602575-15602576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370274063	chr9:15602582-15602583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs80022013	chr9:15602583-15602584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs77873897	chr9:15602584-15602585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374599085	chr9:15602630-15602631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376874817	chr9:15602645-15602646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs199907940	chr9:15602666-15602667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191740387	chr9:15602709-15602710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559128016	chr9:15602734-15602735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545917164	chr9:15602743-15602744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200634103	chr9:15602754-15602755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183867978	chr9:15602758-15602759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15587000-15620400	Weak transcription	Pancreas	Pancrea
2	chr9:15589200-15609800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr9:15589400-15610600	Weak transcription	Thymus	Thymus
4	chr9:15592800-15614000	Weak transcription	Left Ventricle	heart
5	chr9:15599000-15617800	Weak transcription	Aorta	Aorta
6	chr9:15599600-15606200	Weak transcription	Fetal Lung	lung
7	chr9:15600200-15605800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr9:15600200-15614400	Weak transcription	Gastric	stomach
9	chr9:15600600-15617600	Weak transcription	Fetal Stomach	stomach
10	chr9:15601000-15620000	Weak transcription	Ovary	ovary
11	chr9:15601200-15608000	Weak transcription	Fetal Thymus	thymus
12	chr9:15601200-15614000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr9:15601400-15606000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr9:15601600-15605800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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