Variant report

Variant	esv3356308
Chromosome Location	chr12:72985285-72989783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:74 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561489022	chr12:72985296-72985297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542419773	chr12:72985332-72985333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181192889	chr12:72985348-72985349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs657258	chr12:72985409-72985410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199676310	chr12:72985413-72985414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs71071842	chr12:72985427-72985428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547045986	chr12:72985454-72985455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11613390	chr12:72985473-72985474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11179269	chr12:72985521-72985522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562302730	chr12:72985622-72985623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs71458104	chr12:72985626-72985627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186283228	chr12:72985638-72985639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532424662	chr12:72985644-72985645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534782747	chr12:72985671-72985672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550974329	chr12:72985709-72985710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569321579	chr12:72985721-72985722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140368743	chr12:72985769-72985770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531142646	chr12:72985811-72985812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34838567	chr12:72985816-72985817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190666728	chr12:72985842-72985843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1214903	chr12:72985977-72985978	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs564213277	chr12:72986006-72986007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533762940	chr12:72986092-72986093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558749506	chr12:72986134-72986135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35175136	chr12:72986177-72986178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs398098297	chr12:72986180-72986181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570189958	chr12:72986198-72986199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552633808	chr12:72986217-72986218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181606055	chr12:72986261-72986262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555728008	chr12:72986288-72986289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201330085	chr12:72986342-72986343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112791654	chr12:72986344-72986345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554987989	chr12:72986346-72986347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573354522	chr12:72986368-72986369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs662337	chr12:72986414-72986415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377327775	chr12:72986442-72986443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187296303	chr12:72986449-72986450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192137528	chr12:72986474-72986475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566429248	chr12:72986484-72986485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576384867	chr12:72986489-72986490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs398076743	chr12:72986499-72986500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs398044498	chr12:72986500-72986501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182708259	chr12:72986521-72986522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544759170	chr12:72986548-72986549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184992414	chr12:72986554-72986555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144305734	chr12:72986565-72986566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548430713	chr12:72986583-72986584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368801426	chr12:72986595-72986596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535391401	chr12:72986615-72986616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2367748	chr12:72986632-72986633	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Autism	20685689	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	20729466	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:72964400-72986800	Weak transcription	Fetal Intestine Large	intestine
2	chr12:72986800-72987000	Enhancers	Fetal Intestine Large	intestine

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