Variant report

Variant	esv3326795
Chromosome Location	chr2:213208003-213208395
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	chr2:213202563..213204297-chr2:213206010..213208677,2	K562	blood:

Extended variants
information (count: 18 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372398217	chr2:213208004-213208005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs540634067	chr2:213208036-213208037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560083233	chr2:213208040-213208041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532295708	chr2:213208047-213208048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145049867	chr2:213208077-213208078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562378380	chr2:213208101-213208102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573860782	chr2:213208114-213208115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531524816	chr2:213208116-213208117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373467886	chr2:213208146-213208147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367586297	chr2:213208162-213208163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192954689	chr2:213208221-213208222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6754674	chr2:213208256-213208257	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs533611276	chr2:213208289-213208290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547429117	chr2:213208292-213208293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs34672853	chr2:213208296-213208297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570432138	chr2:213208309-213208310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539367079	chr2:213208334-213208335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184981352	chr2:213208359-213208360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	18990708	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213201800-213213000	Weak transcription	Aorta	Aorta
2	chr2:213205600-213221000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:213208000-213210800	Enhancers	Fetal Heart	heart

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