Variant report

Variant	nsv971346
Chromosome Location	chr8:111118125-111121928
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:111121553-111121658	Lung_OC	lung:	n/a	n/a
2	MAFK	chr8:111121831-111122031	HepG2	liver:	n/a	n/a
3	SPI1	chr8:111118062-111118309	HL-60	blood:	n/a	chr8:111118198-111118207 chr8:111118197-111118210

Variant related genes	Relation type
ENSG00000240590	TF binding region

Extended variants
information (count: 20 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556061711	chr8:111118295-111118296	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs150326552	chr8:111118296-111118297	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs534342126	chr8:111121037-111121038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138224087	chr8:111121084-111121085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577924486	chr8:111121085-111121086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544930914	chr8:111121089-111121090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557176863	chr8:111121104-111121105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557334915	chr8:111121174-111121175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573785253	chr8:111121331-111121332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs74853540	chr8:111121341-111121342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190790779	chr8:111121346-111121347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573158579	chr8:111121374-111121375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545510408	chr8:111121647-111121648	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs187233507	chr8:111121839-111121840	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs557115415	chr8:111121856-111121857	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs573871141	chr8:111121867-111121868	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs536464612	chr8:111121882-111121883	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs16880380	chr8:111121885-111121886	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs138831469	chr8:111121892-111121893	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs141922508	chr8:111121924-111121925	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111121000-111121400	Enhancers	Fetal Brain Male	brain

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