Variant report

Variant	esv1573737
Chromosome Location	chr5:127172332-127173282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:127170472..127172876-chr5:127173742..127176446,2	K562	blood:
2	chr5:127172554..127175217-chr5:127418904..127421266,2	K562	blood:

Variant related genes	Relation type
ENSG00000064651	chromatin interactions

Extended variants
information (count: 26 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370538177	chr5:127172333-127172334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373192888	chr5:127172334-127172335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377397362	chr5:127172335-127172336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs367699748	chr5:127172517-127172518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569646316	chr5:127172522-127172523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75708238	chr5:127172531-127172532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529018662	chr5:127172555-127172556	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549954622	chr5:127172634-127172635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs189383524	chr5:127172673-127172674	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs111683181	chr5:127172714-127172715	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs112560227	chr5:127172742-127172743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs76209594	chr5:127172751-127172752	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572293576	chr5:127172815-127172816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs114343398	chr5:127172863-127172864	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201123343	chr5:127172877-127172878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192183176	chr5:127172944-127172945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs112689911	chr5:127172946-127172947	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147095869	chr5:127172972-127172973	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113237919	chr5:127172973-127172974	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112854077	chr5:127172997-127172998	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs111772129	chr5:127173026-127173027	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs184554038	chr5:127173141-127173142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs111383642	chr5:127173234-127173235	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370738376	chr5:127173277-127173278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375697914	chr5:127173279-127173280	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs376419186	chr5:127173280-127173281	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	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
Breast cancer	21858162	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
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	16397240	CNVD
Parathyroid adenoma	22454399	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:127170200-127174400	Weak transcription	NHDF-Ad	bronchial
2	chr5:127170400-127173800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr5:127170400-127180400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr5:127170800-127174600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:127171000-127172600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:127171200-127174400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr5:127171200-127174400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr5:127171400-127174400	Weak transcription	HSMMtube	muscle
9	chr5:127172200-127174400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:127172400-127173000	Weak transcription	HSMM	muscle
11	chr5:127173200-127174200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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