Variant report

Variant	esv3510126
Chromosome Location	chr11:34865674-34866035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34861723..34863511-chr11:34864599..34867573,2	K562	blood:
2	chr11:34865938..34868708-chr11:34870452..34873276,2	K562	blood:
3	chr11:34863977..34866462-chr11:34870377..34873238,2	MCF-7	breast:

Extended variants
information (count: 35 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192721680	chr11:34865777-34865778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140277497	chr11:34865784-34865785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2055805	chr11:34865813-34865814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2055804	chr11:34865817-34865818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538069176	chr11:34865821-34865822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7479677	chr11:34865825-34865826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551469294	chr11:34865828-34865829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12277723	chr11:34865831-34865832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12290799	chr11:34865833-34865834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200592763	chr11:34865834-34865835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs71041944	chr11:34865835-34865836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs60690101	chr11:34865841-34865842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7929545	chr11:34865843-34865844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11606599	chr11:34865845-34865846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs58034710	chr11:34865847-34865848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12277726	chr11:34865849-34865850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11602417	chr11:34865861-34865862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375313869	chr11:34865862-34865863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3980639	chr11:34865863-34865864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs397842098	chr11:34865864-34865865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370771258	chr11:34865867-34865868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371642344	chr11:34865870-34865871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374330498	chr11:34865873-34865874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368407633	chr11:34865877-34865878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12790315	chr11:34865879-34865880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60058800	chr11:34865883-34865884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149027417	chr11:34865887-34865888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7929565	chr11:34865891-34865892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571372823	chr11:34865903-34865904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7932442	chr11:34865907-34865908	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs200277169	chr11:34865910-34865911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201741076	chr11:34865911-34865912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7932461	chr11:34865985-34865986	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs113970072	chr11:34865987-34865988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556842413	chr11:34866022-34866023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34859000-34909400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:34859400-34871800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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