Variant report

Variant	esv32877
Chromosome Location	chr9:116422327-116422643
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	chr9:116420136..116422934-chr9:116424938..116428259,3	K562	blood:
2	chr9:116419179..116421733-chr9:116422325..116423904,2	MCF-7	breast:

Extended variants
information (count: 10 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548718223	chr9:116422350-116422351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114823995	chr9:116422424-116422425	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs10981872	chr9:116422447-116422448	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs139104122	chr9:116422482-116422483	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs545560032	chr9:116422488-116422489	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs547695471	chr9:116422551-116422552	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs568500443	chr9:116422584-116422585	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs10981873	chr9:116422585-116422586	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs531430763	chr9:116422589-116422590	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs140564084	chr9:116422634-116422635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116420200-116425800	Weak transcription	Psoas Muscle	Psoas
2	chr9:116420400-116425800	Weak transcription	Left Ventricle	heart
3	chr9:116420800-116427200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:116421000-116423800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr9:116421000-116425800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr9:116422200-116426000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr9:116422400-116422600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood

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