Variant report

Variant	esv3337433
Chromosome Location	chr7:110303541-110304064
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	chr7:110302721..110305651-chr7:110305918..110310342,3	K562	blood:
2	chr7:110302721..110305651-chr7:110305918..110308870,2	K562	blood:

Extended variants
information (count: 24 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551765923	chr7:110303550-110303551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146216871	chr7:110303552-110303553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571901132	chr7:110303555-110303556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528023605	chr7:110303557-110303558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201919924	chr7:110303629-110303630	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567800193	chr7:110303633-110303634	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368403636	chr7:110303666-110303667	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150558760	chr7:110303679-110303680	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536867048	chr7:110303681-110303682	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200952795	chr7:110303686-110303687	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368781137	chr7:110303702-110303703	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs137966233	chr7:110303711-110303712	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201298424	chr7:110303719-110303720	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536441357	chr7:110303722-110303723	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371793087	chr7:110303723-110303724	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199919844	chr7:110303733-110303734	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542186279	chr7:110303799-110303800	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376432625	chr7:110303816-110303817	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs202079440	chr7:110303828-110303829	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554147736	chr7:110303897-110303898	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534640125	chr7:110303922-110303923	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370603930	chr7:110303941-110303942	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554734164	chr7:110303951-110303952	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76771931	chr7:110304051-110304052	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110301200-110311600	Weak transcription	Pancreas	Pancrea
2	chr7:110302400-110303600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr7:110303600-110303800	ZNF genes & repeats	Aorta	Aorta
4	chr7:110303600-110304600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
5	chr7:110304000-110304200	Weak transcription	Ovary	ovary

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