Variant report

Variant	esv1411144
Chromosome Location	chr5:179868466-179868467
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	BCL3	chr5:179868437-179868959	A549	lung:	n/a	n/a
2	CEBPB	chr5:179868457-179868942	A549	lung:	n/a	n/a
3	CEBPB	chr5:179868404-179869008	Hela-S3	cervix:	n/a	n/a
4	EP300	chr5:179868435-179869042	A549	lung:	n/a	n/a
5	EP300	chr5:179868415-179868939	Hela-S3	cervix:	n/a	n/a
6	FOS	chr5:179868399-179869000	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr5:179868378-179868958	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr5:179868412-179868932	MCF10A-Er-Src	breast:	n/a	n/a
9	MAX	chr5:179868459-179869076	A549	lung:	n/a	n/a
10	MYC	chr5:179868395-179868974	MCF10A-Er-Src	breast:	n/a	n/a
11	MYC	chr5:179868415-179869039	MCF10A-Er-Src	breast:	n/a	n/a
12	RFX5	chr5:179868461-179869018	Hela-S3	cervix:	n/a	n/a
13	STAT3	chr5:179868319-179869101	MCF10A-Er-Src	breast:	n/a	chr5:179868629-179868640 chr5:179868912-179868924
14	STAT3	chr5:179868424-179868827	MCF10A-Er-Src	breast:	n/a	chr5:179868629-179868640
15	STAT3	chr5:179868325-179869001	MCF10A-Er-Src	breast:	n/a	chr5:179868629-179868640 chr5:179868912-179868924
16	STAT3	chr5:179868329-179869050	MCF10A-Er-Src	breast:	n/a	chr5:179868629-179868640 chr5:179868912-179868924
17	STAT3	chr5:179868412-179868922	Hela-S3	cervix:	n/a	chr5:179868629-179868640
18	TBP	chr5:179868444-179869034	Hela-S3	cervix:	n/a	n/a
19	TCF12	chr5:179868431-179869025	A549	lung:	n/a	chr5:179869004-179869011
20	TCF7L2	chr5:179868466-179869057	Hela-S3	cervix:	n/a	n/a

Variant related genes	Relation type
RNU6-525P	TF binding region
ENSG00000250509	TF binding region

Extended variants
information (count: 2 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201142118	chr5:179868466-179868467	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs373850847	chr5:179868467-179868468	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179866000-179869800	Enhancers	Placenta	Placenta
2	chr5:179867200-179868600	Enhancers	A549	lung
3	chr5:179867400-179868800	Weak transcription	Pancreas	Pancrea
4	chr5:179867600-179868800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:179867600-179868800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:179867600-179869000	Enhancers	HepG2	liver
7	chr5:179868400-179868800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr5:179868400-179869200	Enhancers	H1 Cell Line	embryonic stem cell
9	chr5:179868400-179869200	Flanking Active TSS	Hela-S3	cervix

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