Variant report

Variant	esv3487873
Chromosome Location	chr1:62082764-62083782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 94 )

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	rs184223498	chr1:62082796-62082797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7530003	chr1:62082800-62082801	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs576612910	chr1:62082808-62082809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540956678	chr1:62082835-62082836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145479312	chr1:62082875-62082876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs61770645	chr1:62082896-62082897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35279255	chr1:62082931-62082932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142346542	chr1:62083254-62083255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529683637	chr1:62083364-62083365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559947088	chr1:62083418-62083419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550809408	chr1:62083517-62083518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199686795	chr1:62083606-62083607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12138712	chr1:62083691-62083692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144952877	chr1:62083699-62083700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371492068	chr1:62083701-62083702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181104131	chr1:62083706-62083707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563244504	chr1:62083708-62083709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144466147	chr1:62083721-62083722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564783065	chr1:62083748-62083749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145648209	chr1:62083763-62083764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62073200-62084400	Weak transcription	Esophagus	oesophagus
2	chr1:62073200-62086400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:62073200-62098800	Weak transcription	Right Atrium	heart
4	chr1:62073400-62084200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:62079200-62086000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:62080400-62086000	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr1:62080400-62086000	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr1:62080600-62084400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:62081800-62082800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:62081800-62082800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:62081800-62083000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:62082200-62082800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:62082200-62082800	Enhancers	Placenta	Placenta
14	chr1:62082200-62082800	Enhancers	HSMMtube	muscle
15	chr1:62082200-62082800	Enhancers	NHEK	skin
16	chr1:62082200-62083000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:62082400-62082800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr1:62082400-62082800	Enhancers	H1 Cell Line	embryonic stem cell
19	chr1:62082400-62082800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr1:62082400-62082800	Enhancers	HMEC	breast
21	chr1:62082400-62082800	Enhancers	NHDF-Ad	bronchial
22	chr1:62082400-62083200	Weak transcription	Aorta	Aorta
23	chr1:62082800-62083800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr1:62082800-62084000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr1:62082800-62084200	Weak transcription	NHEK	skin
26	chr1:62082800-62084400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:62082800-62084400	Weak transcription	HMEC	breast
28	chr1:62083000-62084200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:62083000-62084200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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