Variant report

Variant	esv3320801
Chromosome Location	chr1:169159960-169160420
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	FOS	chr1:169159801-169160540	HUVEC	blood vessel:	n/a	chr1:169160019-169160028 chr1:169159975-169159986

Variant related genes	Relation type
NME7	TF binding region

Extended variants
information (count: 19 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567611856	chr1:169159983-169159984	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs372278134	chr1:169160031-169160032	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs1209733	chr1:169160037-169160038	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs113393841	chr1:169160040-169160041	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs79708869	chr1:169160058-169160059	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs540219040	chr1:169160090-169160091	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs529689787	chr1:169160140-169160141	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs1200081	chr1:169160176-169160177	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
9	rs12078340	chr1:169160181-169160182	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs573785324	chr1:169160209-169160210	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs544256592	chr1:169160255-169160256	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs563338560	chr1:169160267-169160268	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs61806212	chr1:169160302-169160303	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs545794319	chr1:169160343-169160344	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs564389850	chr1:169160344-169160345	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs528119939	chr1:169160345-169160346	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs546613829	chr1:169160348-169160349	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs189707046	chr1:169160349-169160350	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs34321069	chr1:169160409-169160410	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169130400-169195200	Weak transcription	Pancreas	Pancrea
2	chr1:169150400-169162600	Weak transcription	Psoas Muscle	Psoas
3	chr1:169155600-169162800	Weak transcription	A549	lung
4	chr1:169158000-169162200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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