Variant report

Variant	esv1198553
Chromosome Location	chr17:17210839-17210955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:17206364..17208398-chr17:17209941..17213545,3	K562	blood:
2	chr17:17208801..17211500-chr17:17212321..17214935,3	K562	blood:
3	chr17:17208563..17211113-chr17:17230202..17232936,2	K562	blood:
4	chr17:17210615..17212933-chr17:17216145..17218619,3	K562	blood:
5	chr17:17209561..17211178-chr17:17215643..17218220,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000205309	chromatin interactions

Extended variants
information (count: 15 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12951983	chr17:17210840-17210841	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12951985	chr17:17210841-17210842	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs180779848	chr17:17210849-17210850	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs12951504	chr17:17210851-17210852	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs12951519	chr17:17210869-17210870	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs12951289	chr17:17210873-17210874	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs190862945	chr17:17210881-17210882	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs12936127	chr17:17210882-17210883	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs183896528	chr17:17210883-17210884	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs188937418	chr17:17210884-17210885	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs190629722	chr17:17210892-17210893	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs146887220	chr17:17210895-17210896	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140482286	chr17:17210896-17210897	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs9903425	chr17:17210903-17210904	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs532096449	chr17:17210908-17210909	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:160)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	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
Adenoid cystic carcinoma	18332873	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	21811587	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
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric cancer	18160780	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
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22543975	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17207400-17215000	Weak transcription	Ovary	ovary
2	chr17:17207400-17235400	Weak transcription	Lung	lung
3	chr17:17207600-17217800	Weak transcription	Stomach Smooth Muscle	stomach
4	chr17:17207600-17246400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr17:17207800-17211200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr17:17207800-17212800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr17:17207800-17215000	Weak transcription	Fetal Lung	lung
8	chr17:17207800-17216600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr17:17207800-17216800	Weak transcription	Fetal Intestine Large	intestine
10	chr17:17207800-17226400	Weak transcription	Brain Angular Gyrus	brain
11	chr17:17207800-17228000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr17:17207800-17228000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr17:17207800-17228400	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr17:17207800-17229600	Weak transcription	Adipose Nuclei	Adipose
15	chr17:17207800-17243400	Weak transcription	Colon Smooth Muscle	Colon
16	chr17:17208000-17216800	Weak transcription	Left Ventricle	heart
17	chr17:17208000-17218600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr17:17208000-17226000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr17:17208000-17226200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr17:17208200-17213600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr17:17208200-17214800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr17:17208200-17216600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr17:17208200-17216800	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr17:17208200-17225400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr17:17208200-17225400	Weak transcription	Brain Anterior Caudate	brain
26	chr17:17208200-17226400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr17:17208200-17228200	Weak transcription	Brain Hippocampus Middle	brain
28	chr17:17208400-17212000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr17:17208400-17216800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr17:17208400-17225400	Weak transcription	Brain Germinal Matrix	brain
31	chr17:17208600-17255400	Weak transcription	Brain Substantia Nigra	brain
32	chr17:17208800-17236000	Weak transcription	Right Ventricle	heart
33	chr17:17209000-17211000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr17:17209000-17217600	Weak transcription	Rectal Smooth Muscle	rectum
35	chr17:17209000-17226000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr17:17209000-17227600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr17:17209200-17212000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr17:17209200-17212000	Weak transcription	Fetal Brain Male	brain
39	chr17:17209200-17212400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr17:17209200-17212400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr17:17209200-17215000	Weak transcription	Fetal Brain Female	brain
42	chr17:17209200-17224000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr17:17209200-17224600	Weak transcription	Fetal Muscle Trunk	muscle
44	chr17:17209400-17216800	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr17:17209600-17217000	Weak transcription	Fetal Heart	heart
46	chr17:17209800-17213600	Weak transcription	Dnd41	blood
47	chr17:17209800-17216800	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr17:17209800-17216800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr17:17209800-17216800	Weak transcription	A549	lung
50	chr17:17209800-17217800	Weak transcription	Thymus	Thymus

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