Variant report

Variant	esv3401631
Chromosome Location	chr11:34047772-34048482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34046638..34048627-chr11:34065248..34067644,2	MCF-7	breast:
2	chr11:34040788..34042322-chr11:34047509..34050356,2	K562	blood:
3	chr11:34047888..34049807-chr11:34058557..34060291,2	K562	blood:
4	chr11:34044990..34047866-chr11:34056596..34058882,2	K562	blood:

Extended variants
information (count: 83 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:83 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11032493	chr11:34047777-34047778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372929000	chr11:34047794-34047795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11032494	chr11:34047802-34047803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11032495	chr11:34047807-34047808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146653432	chr11:34047825-34047826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139062932	chr11:34047835-34047836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533601669	chr11:34047850-34047851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188624865	chr11:34047859-34047860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561845909	chr11:34047867-34047868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149904795	chr11:34047868-34047869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11600775	chr11:34047874-34047875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs61880366	chr11:34047877-34047878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs145611051	chr11:34047909-34047910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75540078	chr11:34047912-34047913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528651788	chr11:34047945-34047946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548966849	chr11:34047950-34047951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375801526	chr11:34047953-34047954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568955699	chr11:34047960-34047961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192908207	chr11:34047963-34047964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149080966	chr11:34047965-34047966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576938197	chr11:34047968-34047969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145915146	chr11:34047970-34047971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147829450	chr11:34048000-34048001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141387454	chr11:34048003-34048004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542193633	chr11:34048020-34048021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183107811	chr11:34048021-34048022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370493331	chr11:34048026-34048027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374580794	chr11:34048049-34048050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370741816	chr11:34048060-34048061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368115093	chr11:34048062-34048063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374071179	chr11:34048063-34048064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372297783	chr11:34048064-34048065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368399283	chr11:34048067-34048068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201492300	chr11:34048072-34048073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200078836	chr11:34048079-34048080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374617694	chr11:34048085-34048086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201266555	chr11:34048086-34048087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187228060	chr11:34048115-34048116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575348053	chr11:34048120-34048121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544302843	chr11:34048121-34048122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150425070	chr11:34048134-34048135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111218952	chr11:34048140-34048141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138190518	chr11:34048146-34048147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111218989	chr11:34048152-34048153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149594631	chr11:34048159-34048160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146108394	chr11:34048164-34048165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568894482	chr11:34048170-34048171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368499499	chr11:34048186-34048187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140135442	chr11:34048194-34048195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375262655	chr11:34048197-34048198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34041400-34048800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:34046600-34049400	Weak transcription	Aorta	Aorta
3	chr11:34047600-34048800	Weak transcription	Fetal Intestine Small	intestine
4	chr11:34047800-34048800	Weak transcription	Liver	Liver

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