Variant report

Variant	nsv551859
Chromosome Location	chr10:90944216-90947171
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:90807595..90810361-chr10:90944518..90946449,2	MCF-7	breast:

Extended variants
information (count: 103 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:103 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4269843	chr10:90944216-90944217	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188824169	chr10:90944267-90944268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73368250	chr10:90944294-90944295	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs559932494	chr10:90944307-90944308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530195523	chr10:90944317-90944318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535627100	chr10:90944344-90944345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147572334	chr10:90944407-90944408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570000224	chr10:90944437-90944438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149034928	chr10:90944441-90944442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11203016	chr10:90944472-90944473	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs570322068	chr10:90944513-90944514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79124621	chr10:90944530-90944531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552748649	chr10:90944531-90944532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567347699	chr10:90944547-90944548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116062622	chr10:90944627-90944628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535520337	chr10:90944644-90944645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10788636	chr10:90944659-90944660	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs34137383	chr10:90944708-90944709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142193209	chr10:90944796-90944797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs180851463	chr10:90944820-90944821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541516336	chr10:90944886-90944887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs74821185	chr10:90944894-90944895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs377743565	chr10:90944915-90944916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374299647	chr10:90944925-90944926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs151227281	chr10:90944983-90944984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114005928	chr10:90944998-90944999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs367591337	chr10:90945005-90945006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183968341	chr10:90945018-90945019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564494989	chr10:90945021-90945022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530150373	chr10:90945024-90945025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542282050	chr10:90945037-90945038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35064463	chr10:90945076-90945077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563537305	chr10:90945108-90945109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188302083	chr10:90945167-90945168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552281797	chr10:90945181-90945182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570462118	chr10:90945206-90945207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140282114	chr10:90945212-90945213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546425162	chr10:90945279-90945280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150357904	chr10:90945349-90945350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77230444	chr10:90945359-90945360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368183151	chr10:90945396-90945397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556975457	chr10:90945442-90945443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76937316	chr10:90945465-90945466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs578046583	chr10:90945513-90945514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138866060	chr10:90945516-90945517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140634288	chr10:90945523-90945524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145701301	chr10:90945531-90945532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562595776	chr10:90945535-90945536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553625759	chr10:90945558-90945559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574929803	chr10:90945585-90945586	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90943200-90944400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr10:90943600-90945000	Enhancers	Osteobl	bone
3	chr10:90943800-90945400	Weak transcription	NHLF	lung
4	chr10:90944000-90945200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr10:90944400-90949400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr10:90945200-90945800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr10:90945200-90946000	Enhancers	Stomach Smooth Muscle	stomach
8	chr10:90945400-90945600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr10:90945400-90945800	Enhancers	Duodenum Smooth Muscle	Duodenum
10	chr10:90945400-90945800	Enhancers	Hela-S3	cervix
11	chr10:90945400-90946600	Enhancers	Fetal Lung	lung
12	chr10:90945600-90945800	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr10:90945600-90945800	Enhancers	NHLF	lung
14	chr10:90945600-90946000	Enhancers	Colon Smooth Muscle	Colon
15	chr10:90945600-90946000	Bivalent Enhancer	Stomach Mucosa	stomach
16	chr10:90946200-90947200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr10:90946400-90946800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr10:90946400-90947000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr10:90946400-90947000	Enhancers	H9 Cell Line	embryonic stem cell

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