Variant report

Variant	nsv8366
Chromosome Location	chr8:91190052-91195338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:91190260..91192251-chr8:91205033..91207499,2	K562	blood:
2	chr8:91180613..91183439-chr8:91193363..91195732,2	K562	blood:
3	chr8:91187662..91190502-chr8:91236582..91238750,2	K562	blood:
4	chr8:91182635..91184941-chr8:91189567..91191174,2	MCF-7	breast:
5	chr8:91193596..91196582-chr8:91200011..91201961,3	K562	blood:
6	chr8:91186935..91188480-chr8:91190108..91192578,2	MCF-7	breast:
7	chr8:91177720..91183484-chr8:91189779..91192790,4	K562	blood:
8	chr8:91193596..91196355-chr8:91200011..91201961,2	K562	blood:
9	chr8:91195100..91196918-chr8:91207528..91209221,2	K562	blood:

No data

Extended variants
information (count: 221 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:221 , 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	rs186717289	chr8:91190055-91190056	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs571670996	chr8:91190063-91190064	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs550955972	chr8:91190096-91190097	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs369256508	chr8:91190129-91190130	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs569290694	chr8:91190181-91190182	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs539913582	chr8:91190204-91190205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2214417	chr8:91190214-91190215	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs573341147	chr8:91190222-91190223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139300928	chr8:91190267-91190268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190225754	chr8:91190276-91190277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370451197	chr8:91190295-91190296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2189255	chr8:91190297-91190298	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs555709551	chr8:91190305-91190306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577245792	chr8:91190311-91190312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2189256	chr8:91190322-91190323	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs142899710	chr8:91190334-91190335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs5893119	chr8:91190337-91190338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527494053	chr8:91190386-91190387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183123417	chr8:91190443-91190444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560937739	chr8:91190518-91190519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35549178	chr8:91190552-91190553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562895464	chr8:91190563-91190564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554874497	chr8:91190625-91190626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73307919	chr8:91190685-91190686	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs200155044	chr8:91190774-91190775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201324848	chr8:91190776-91190777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199554896	chr8:91190777-91190778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs199912299	chr8:91190778-91190779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs28391407	chr8:91190779-91190780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35180283	chr8:91190780-91190781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551575467	chr8:91190781-91190782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146118195	chr8:91190811-91190812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs6994103	chr8:91190824-91190825	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs145742492	chr8:91190831-91190832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529115765	chr8:91190861-91190862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs76051629	chr8:91191014-91191015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7011436	chr8:91191015-91191016	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs576866185	chr8:91191069-91191070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556470751	chr8:91191070-91191071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540806945	chr8:91191104-91191105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187463404	chr8:91191114-91191115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140138349	chr8:91191168-91191169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143873334	chr8:91191181-91191182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542374582	chr8:91191219-91191220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561109245	chr8:91191296-91191297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531566558	chr8:91191303-91191304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7013238	chr8:91191332-91191333	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs565219925	chr8:91191358-91191359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11776764	chr8:91191365-91191366	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs551711353	chr8:91191366-91191367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91189000-91190200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:91189000-91190800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:91189800-91190200	Flanking Active TSS	K562	blood
4	chr8:91190000-91190200	Enhancers	Fetal Brain Male	brain
5	chr8:91190000-91190600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:91190200-91191000	Enhancers	K562	blood
7	chr8:91191000-91191400	Weak transcription	K562	blood
8	chr8:91191400-91192000	Enhancers	K562	blood
9	chr8:91192000-91193000	Weak transcription	K562	blood
10	chr8:91193000-91195200	Enhancers	K562	blood
11	chr8:91195200-91196800	Weak transcription	K562	blood

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