Variant report

Variant	esv6951
Chromosome Location	chr5:119379918-119382903
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:52 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534725456	chr5:119379934-119379935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558640119	chr5:119379944-119379945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371547422	chr5:119379954-119379955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs13163408	chr5:119380060-119380061	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs540924220	chr5:119380076-119380077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559257058	chr5:119380081-119380082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs56788223	chr5:119380132-119380133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182471349	chr5:119380134-119380135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72663339	chr5:119380147-119380148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531947647	chr5:119380149-119380150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551724006	chr5:119380150-119380151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571695328	chr5:119380152-119380153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189186545	chr5:119380165-119380166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574408199	chr5:119380225-119380226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547806275	chr5:119380419-119380420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567673877	chr5:119380420-119380421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536504944	chr5:119380489-119380490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146096361	chr5:119381014-119381015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370853064	chr5:119381080-119381081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138944579	chr5:119381128-119381129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191838456	chr5:119381290-119381291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572097552	chr5:119381319-119381320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149233877	chr5:119381441-119381442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112847676	chr5:119381491-119381492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558013555	chr5:119381588-119381589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574114471	chr5:119381678-119381679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs563144116	chr5:119381755-119381756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542876720	chr5:119381794-119381795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143446865	chr5:119381856-119381857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183105496	chr5:119381910-119381911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376335589	chr5:119382002-119382003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148006572	chr5:119382011-119382012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545583253	chr5:119382090-119382091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565382108	chr5:119382138-119382139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141703771	chr5:119382149-119382150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547915494	chr5:119382171-119382172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146359661	chr5:119382193-119382194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530480330	chr5:119382207-119382208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs578215739	chr5:119382295-119382296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549942416	chr5:119382329-119382330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73792818	chr5:119382361-119382362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569928117	chr5:119382382-119382383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1209530	chr5:119382496-119382497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552287257	chr5:119382545-119382546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187355254	chr5:119382653-119382654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372132317	chr5:119382680-119382681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528119486	chr5:119382729-119382730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548097111	chr5:119382751-119382752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537647285	chr5:119382807-119382808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191813300	chr5:119382839-119382840	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119379200-119380200	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr5:119380200-119382600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr5:119382600-119383200	Enhancers	Primary neutrophils fromperipheralblood	blood

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