Variant report

Variant	esv3390217
Chromosome Location	chr7:85089685-85089855
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11983508	chr7:85089685-85089686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190840956	chr7:85089707-85089708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529805473	chr7:85089709-85089710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11979897	chr7:85089723-85089724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547122310	chr7:85089724-85089725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559022384	chr7:85089725-85089726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs13244267	chr7:85089731-85089732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs13229892	chr7:85089733-85089734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534512796	chr7:85089734-85089735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13244271	chr7:85089739-85089740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376264788	chr7:85089740-85089741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113220808	chr7:85089742-85089743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138391081	chr7:85089757-85089758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13232878	chr7:85089762-85089763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13232585	chr7:85089768-85089769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs13232671	chr7:85089771-85089772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13247045	chr7:85089777-85089778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374620570	chr7:85089779-85089780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368197255	chr7:85089790-85089791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533000902	chr7:85089791-85089792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142466152	chr7:85089807-85089808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374276629	chr7:85089815-85089816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13311931	chr7:85089817-85089818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373019212	chr7:85089818-85089819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs202181719	chr7:85089826-85089827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183916744	chr7:85089835-85089836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:85082400-85090800	Weak transcription	Fetal Stomach	stomach

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