Variant report

Variant	esv3407929
Chromosome Location	chr15:31802653-31803111
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368111901	chr15:31802675-31802676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs141957620	chr15:31802710-31802711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200849637	chr15:31802711-31802712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146020950	chr15:31802714-31802715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186457925	chr15:31802718-31802719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563544183	chr15:31802733-31802734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531396819	chr15:31802739-31802740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577226860	chr15:31802743-31802744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549626935	chr15:31802747-31802748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374634048	chr15:31802763-31802764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62004092	chr15:31802764-31802765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545970317	chr15:31802779-31802780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371739641	chr15:31802788-31802789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79518052	chr15:31802789-31802790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62637726	chr15:31802814-31802815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs62637727	chr15:31802839-31802840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561699722	chr15:31802859-31802860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74196609	chr15:31802864-31802865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71474665	chr15:31802889-31802890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368603408	chr15:31802963-31802964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191305353	chr15:31802989-31802990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553461960	chr15:31802993-31802994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148467602	chr15:31803014-31803015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182729498	chr15:31803016-31803017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528864091	chr15:31803022-31803023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542260380	chr15:31803030-31803031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139098161	chr15:31803039-31803040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186864827	chr15:31803041-31803042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530832010	chr15:31803055-31803056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372025878	chr15:31803061-31803062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150960453	chr15:31803064-31803065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564120223	chr15:31803071-31803072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374851234	chr15:31803083-31803084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372634798	chr15:31803084-31803085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201109044	chr15:31803087-31803088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143389702	chr15:31803088-31803089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142481627	chr15:31803090-31803091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533202075	chr15:31803093-31803094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111154300	chr15:31803099-31803100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369974532	chr15:31803107-31803108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566262254	chr15:31803110-31803111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31782400-31821000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr15:31787200-31810800	Weak transcription	Pancreas	Pancrea
3	chr15:31797000-31814200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr15:31802600-31802800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr15:31802600-31804200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr15:31802600-31804200	Weak transcription	Psoas Muscle	Psoas
7	chr15:31802600-31814200	Weak transcription	Brain Hippocampus Middle	brain
8	chr15:31802600-31814400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr15:31802600-31814400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr15:31802600-31817000	Weak transcription	Brain Angular Gyrus	brain
11	chr15:31802600-31817000	Weak transcription	Brain Substantia Nigra	brain
12	chr15:31802600-31817200	Weak transcription	Brain Anterior Caudate	brain
13	chr15:31802600-31825200	Weak transcription	Fetal Brain Female	brain

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