Variant report

Variant	nsv982634
Chromosome Location	chr9:7584179-7592837
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr9:7592689-7592696	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr9:7592740-7592890	HFF	foreskin:	n/a	chr9:7592820-7592828
3	CTCF	chr9:7592760-7592910	HepG2	liver:	n/a	chr9:7592820-7592828
4	CTCF	chr9:7592760-7592910	HRPEpiC	eye:	n/a	chr9:7592820-7592828
5	CTCF	chr9:7592760-7592910	HCT-116	colon:	n/a	chr9:7592820-7592828
6	CTCF	chr9:7592820-7592970	HFF-Myc	foreskin:	n/a	chr9:7592820-7592828
7	CTCF	chr9:7592700-7592850	HAc	cerebellar:	n/a	chr9:7592820-7592828
8	CTCF	chr9:7592760-7592910	GM12869	blood:	n/a	chr9:7592820-7592828
9	CTCF	chr9:7592700-7592850	GM12865	blood:	n/a	chr9:7592820-7592828
10	CTCF	chr9:7592740-7592890	GM12874	blood:	n/a	chr9:7592820-7592828
11	CTCF	chr9:7592760-7592910	SK-N-SH_RA	brain:	n/a	chr9:7592820-7592828
12	CTCF	chr9:7592800-7592950	GM12875	blood:	n/a	chr9:7592820-7592828
13	CTCF	chr9:7592760-7592910	AoAF	blood vessel:	n/a	chr9:7592820-7592828
14	CTCF	chr9:7592620-7592770	NB4	blood:	n/a	n/a
15	CTCF	chr9:7592680-7592830	GM12865	blood:	n/a	chr9:7592820-7592828
16	CTCF	chr9:7592720-7592870	GM12870	blood:	n/a	chr9:7592820-7592828
17	CTCF	chr9:7592700-7592850	GM12875	blood:	n/a	chr9:7592820-7592828
18	CTCF	chr9:7592780-7592930	NHEK	skin:	n/a	chr9:7592820-7592828
19	CTCF	chr9:7592760-7592910	A549	lung:	n/a	chr9:7592820-7592828
20	CTCF	chr9:7592825-7592906	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr9:7592820-7592970	HMF	breast:	n/a	chr9:7592820-7592828
22	CTCF	chr9:7592804-7592901	Spleen_OC	spleen:	n/a	chr9:7592820-7592828
23	CTCF	chr9:7592680-7592830	HA-sp	spinal cord:	n/a	chr9:7592820-7592828
24	CTCF	chr9:7592720-7592870	Caco-2	colon:	n/a	chr9:7592820-7592828
25	CTCF	chr9:7592820-7592970	HAc	cerebellar:	n/a	chr9:7592820-7592828
26	CTCF	chr9:7592720-7592870	HRE	kidney:	n/a	chr9:7592820-7592828
27	CTCF	chr9:7592720-7592870	HMEC	breast:	n/a	chr9:7592820-7592828
28	CTCF	chr9:7592760-7592910	GM12878	blood:	n/a	chr9:7592820-7592828
29	CTCF	chr9:7592648-7593010	H1-hESC	embryonic stem cell:	n/a	chr9:7592820-7592828
30	CTCF	chr9:7592700-7592850	GM12866	blood:	n/a	chr9:7592820-7592828
31	CTCF	chr9:7592760-7592910	HUVEC	blood vessel:	n/a	chr9:7592820-7592828
32	CTCF	chr9:7592788-7592908	HUVEC	blood vessel:	n/a	chr9:7592820-7592828
33	CTCF	chr9:7592780-7592930	AG04450	lung:	n/a	chr9:7592820-7592828
34	CTCF	chr9:7592760-7592910	HEK293	kidney:	n/a	chr9:7592820-7592828
35	CTCF	chr9:7592780-7592930	Caco-2	colon:	n/a	chr9:7592820-7592828
36	CTCF	chr9:7592784-7592863	GM12878	blood:	n/a	chr9:7592820-7592828
37	CTCF	chr9:7592740-7592890	GM12868	blood:	n/a	chr9:7592820-7592828
38	CTCF	chr9:7592780-7592930	HEK293	kidney:	n/a	chr9:7592820-7592828
39	CTCF	chr9:7592802-7592806	HepG2	liver:	n/a	n/a
40	CTCF	chr9:7592740-7592890	HBMEC	blood vessel:	n/a	chr9:7592820-7592828
41	CTCF	chr9:7592800-7592950	SK-N-SH_RA	brain:	n/a	chr9:7592820-7592828
42	CTCF	chr9:7592780-7592930	HEEpiC	esophagus:	n/a	chr9:7592820-7592828
43	CTCF	chr9:7592760-7592910	MCF-7	breast:	n/a	chr9:7592820-7592828
44	CTCF	chr9:7592742-7592922	MCF-7	breast:	n/a	chr9:7592820-7592828
45	CTCF	chr9:7592760-7592910	GM12873	blood:	n/a	chr9:7592820-7592828
46	CTCF	chr9:7592680-7592830	BE2_C	brain:	n/a	chr9:7592820-7592828
47	CTCF	chr9:7592760-7592910	HBMEC	blood vessel:	n/a	chr9:7592820-7592828
48	CTCF	chr9:7592760-7592910	GM12872	blood:	n/a	chr9:7592820-7592828
49	CTCF	chr9:7592700-7592850	GM12867	blood:	n/a	chr9:7592820-7592828
50	CTCF	chr9:7592800-7592950	GM12864	blood:	n/a	chr9:7592820-7592828

No.	Distal block	Cell Line	Cell type
1	chr1:121484531..121485420-chr9:7590895..7591415,3	MCF-7	breast:
2	chr9:7592716..7593255-chr9:7844122..7844707,2	MCF-7	breast:
3	chr9:7579179..7582103-chr9:7582391..7584856,2	K562	blood:
4	chr9:7592774..7593282-chr9:7827299..7827877,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000178654	TF binding region

Extended variants
information (count: 21 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3852399	chr9:7592407-7592408	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185017482	chr9:7592413-7592414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114012391	chr9:7592427-7592428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188405997	chr9:7592489-7592490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565496595	chr9:7592503-7592504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532649250	chr9:7592514-7592515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs146431128	chr9:7592536-7592537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562133206	chr9:7592554-7592555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376841599	chr9:7592589-7592590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529671165	chr9:7592590-7592591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547866955	chr9:7592597-7592598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566411307	chr9:7592598-7592599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527402768	chr9:7592623-7592624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562046648	chr9:7592638-7592639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs80248175	chr9:7592639-7592640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570638562	chr9:7592667-7592668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143087472	chr9:7592670-7592671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545920924	chr9:7592735-7592736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569250625	chr9:7592787-7592788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs386732251	chr9:7592809-7592810	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs115132042	chr9:7592810-7592811	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7592400-7593000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:7592400-7593200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr9:7592600-7592800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr9:7592600-7593200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:7592600-7593200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr9:7592600-7593200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr9:7592800-7593200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr9:7592800-7593200	Active TSS	iPS-20b Cell Line	embryonic stem cell

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