Variant report

Variant	esv3396628
Chromosome Location	chr19:44292344-44292474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:44235650..44238145-chr19:44290360..44292813,2	K562	blood:
2	chr19:44267187..44269964-chr19:44291691..44294557,2	MCF-7	breast:
3	chr19:44289645..44292572-chr19:44300661..44302875,2	MCF-7	breast:
4	chr19:44287294..44289449-chr19:44292434..44295257,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000159871	chromatin interactions
ENSG00000105771	chromatin interactions

Extended variants
information (count: 21 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546406206	chr19:44292377-44292378	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs566202995	chr19:44292381-44292382	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs182379357	chr19:44292391-44292392	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs187867324	chr19:44292394-44292395	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs375266275	chr19:44292405-44292406	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs58699985	chr19:44292408-44292409	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs371315989	chr19:44292409-44292410	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs376736995	chr19:44292411-44292412	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369789395	chr19:44292413-44292414	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs55762280	chr19:44292415-44292416	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs57957955	chr19:44292418-44292419	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs10427133	chr19:44292442-44292443	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs372511891	chr19:44292448-44292449	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs375630029	chr19:44292450-44292451	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs369525933	chr19:44292451-44292452	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs373933796	chr19:44292453-44292454	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs60351994	chr19:44292454-44292455	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs59568769	chr19:44292462-44292463	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs57668594	chr19:44292466-44292467	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs184498060	chr19:44292470-44292471	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs60259939	chr19:44292474-44292475	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:44289400-44302600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr19:44289600-44293000	Weak transcription	GM12878-XiMat	blood
3	chr19:44289600-44294800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr19:44289600-44295400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:44289800-44300800	Weak transcription	Placenta	Placenta
6	chr19:44290000-44302400	Weak transcription	NHEK	skin
7	chr19:44290200-44302200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr19:44291400-44293200	Weak transcription	HMEC	breast

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