Variant report

Variant	esv3504706
Chromosome Location	chr17:19571853-19572371
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	chr17:19569611..19572312-chr17:19574479..19577295,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000072210	chromatin interactions

Extended variants
information (count: 24 )
Associated
traits (count: 152 )

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117918589	chr17:19571874-19571875	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs539969803	chr17:19571890-19571891	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs553526324	chr17:19571893-19571894	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192511973	chr17:19571894-19571895	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375802303	chr17:19571911-19571912	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369619837	chr17:19571912-19571913	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs148788408	chr17:19571931-19571932	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575540273	chr17:19572004-19572005	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541641922	chr17:19572016-19572017	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577959985	chr17:19572020-19572021	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs543013550	chr17:19572023-19572024	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs142278193	chr17:19572059-19572060	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs181849605	chr17:19572070-19572071	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs116413888	chr17:19572071-19572072	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs532865911	chr17:19572091-19572092	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs151236073	chr17:19572136-19572137	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs139514139	chr17:19572146-19572147	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs528817295	chr17:19572191-19572192	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs367709733	chr17:19572192-19572193	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs35265843	chr17:19572276-19572277	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs149750446	chr17:19572280-19572281	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs372202442	chr17:19572320-19572321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568652084	chr17:19572345-19572346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550517332	chr17:19572367-19572368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:152)

Disease	PMID	Source
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Autism	22543975	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19553200-19577400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr17:19553200-19580000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr17:19554800-19574400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr17:19555000-19581800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr17:19555000-19582800	Weak transcription	HUVEC	blood vessel
6	chr17:19555200-19576400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr17:19555600-19578600	Weak transcription	Small Intestine	intestine
8	chr17:19558400-19579200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr17:19559200-19574200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr17:19559400-19575000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr17:19559400-19575400	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr17:19559600-19578600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr17:19559800-19577200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr17:19564000-19581000	Weak transcription	Thymus	Thymus
15	chr17:19564800-19574600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr17:19565400-19575800	Strong transcription	Fetal Stomach	stomach
17	chr17:19567000-19575800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr17:19567400-19574400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr17:19567400-19574400	Weak transcription	Fetal Heart	heart
20	chr17:19567400-19574800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr17:19567600-19574400	Weak transcription	Primary B cells from cord blood	blood
22	chr17:19567600-19574400	Weak transcription	Stomach Mucosa	stomach
23	chr17:19567600-19578600	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr17:19567600-19584800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr17:19567800-19572800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr17:19567800-19574600	Weak transcription	NHDF-Ad	bronchial
27	chr17:19567800-19575200	Weak transcription	HSMM	muscle
28	chr17:19567800-19578600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr17:19568400-19573200	Strong transcription	Skeletal Muscle Female	skeletal muscle
30	chr17:19568400-19574400	Weak transcription	Right Atrium	heart
31	chr17:19568400-19574600	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr17:19568400-19574600	Weak transcription	Hela-S3	cervix
33	chr17:19568400-19574800	Weak transcription	Osteobl	bone
34	chr17:19568400-19581800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr17:19568600-19574200	Weak transcription	Primary B cells from peripheral blood	blood
36	chr17:19568600-19575200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr17:19568600-19606800	Weak transcription	Psoas Muscle	Psoas
38	chr17:19568800-19572800	Weak transcription	Primary T cells from cord blood	blood
39	chr17:19569000-19582000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr17:19569200-19574400	Weak transcription	Primary hematopoietic stem cells	blood
41	chr17:19569200-19574400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr17:19569400-19572800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr17:19569400-19573000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr17:19569400-19574000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr17:19569400-19574200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr17:19569400-19574200	Weak transcription	HSMMtube	muscle
47	chr17:19569400-19574400	Weak transcription	Left Ventricle	heart
48	chr17:19569400-19577000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr17:19569600-19573200	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr17:19569600-19574000	Weak transcription	Brain Hippocampus Middle	brain

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