Variant report

Variant	esv3340470
Chromosome Location	chr18:28070104-28072752
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 238 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:238 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8089627	chr18:28070122-28070123	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377223645	chr18:28070125-28070126	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs117942043	chr18:28070154-28070155	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556337837	chr18:28070157-28070158	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558806977	chr18:28070161-28070162	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77838199	chr18:28070183-28070184	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114759936	chr18:28070186-28070187	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs74657598	chr18:28070194-28070195	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs78956087	chr18:28070197-28070198	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542151606	chr18:28070200-28070201	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139083987	chr18:28070232-28070233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144058028	chr18:28070286-28070287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545753288	chr18:28070305-28070306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564040106	chr18:28070309-28070310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113320898	chr18:28070312-28070313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535642840	chr18:28070314-28070315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114728213	chr18:28070322-28070323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550001824	chr18:28070351-28070352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146484259	chr18:28070361-28070362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139940254	chr18:28070382-28070383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193186639	chr18:28070410-28070411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565937278	chr18:28070455-28070456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533956556	chr18:28070460-28070461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185078963	chr18:28070499-28070500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190817697	chr18:28070505-28070506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113048822	chr18:28070511-28070512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530051495	chr18:28070512-28070513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537949125	chr18:28070513-28070514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556382077	chr18:28070523-28070524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368682793	chr18:28070533-28070534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371804528	chr18:28070544-28070545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369259820	chr18:28070548-28070549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371785022	chr18:28070550-28070551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375174834	chr18:28070555-28070556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375157057	chr18:28070558-28070559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369654316	chr18:28070560-28070561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373850088	chr18:28070561-28070562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377013229	chr18:28070568-28070569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369026047	chr18:28070569-28070570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372637713	chr18:28070571-28070572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572770705	chr18:28070572-28070573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370648099	chr18:28070574-28070575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375414523	chr18:28070580-28070581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377636411	chr18:28070582-28070583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371046001	chr18:28070597-28070598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375434540	chr18:28070605-28070606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368706735	chr18:28070609-28070610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371668681	chr18:28070616-28070617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376238391	chr18:28070631-28070632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371672191	chr18:28070637-28070638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28066800-28073800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr18:28069600-28070200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr18:28069600-28070200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr18:28069800-28070200	Enhancers	K562	blood
5	chr18:28069800-28070400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr18:28069800-28070400	Enhancers	Placenta Amnion	Placenta Amnion
7	chr18:28069800-28070400	Enhancers	NHEK	skin
8	chr18:28070000-28070200	Genic enhancers	HMEC	breast
9	chr18:28070200-28070400	Enhancers	HSMM	muscle
10	chr18:28070200-28071600	Weak transcription	HMEC	breast
11	chr18:28070200-28073800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr18:28072000-28072200	Enhancers	K562	blood

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