Variant report

Variant	esv1936908
Chromosome Location	chr4:78199050-78199464
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 74 )

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	rs184095614	chr4:78199146-78199147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541765944	chr4:78199174-78199175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571646272	chr4:78199183-78199184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548918130	chr4:78199192-78199193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145913869	chr4:78199194-78199195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117567863	chr4:78199206-78199207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs55954324	chr4:78199207-78199208	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs79977653	chr4:78199215-78199216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs59408083	chr4:78199226-78199227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs386676318	chr4:78199260-78199261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112956315	chr4:78199270-78199271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148138408	chr4:78199284-78199285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141972318	chr4:78199285-78199286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs28483113	chr4:78199304-78199305	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs576838837	chr4:78199330-78199331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372927910	chr4:78199355-78199356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187313580	chr4:78199361-78199362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9995518	chr4:78199379-78199380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs4141661	chr4:78199437-78199438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115249447	chr4:78199459-78199460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78191000-78200000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:78193600-78205400	Weak transcription	Placenta	Placenta

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