Variant report

Variant	nsv1000371
Chromosome Location	chr3:42355114-42372639
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:29)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:29 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr3:42355882-42356211	HCT-116	colon:	n/a	n/a
2	CBX3	chr3:42355930-42356190	K562	blood:	n/a	n/a
3	CBX3	chr3:42358618-42358971	HCT-116	colon:	n/a	n/a
4	CBX3	chr3:42355881-42356307	HCT-116	colon:	n/a	n/a
5	FOXA2	chr3:42370653-42370857	HepG2	liver:	n/a	n/a
6	GATA3	chr3:42370680-42370779	SH-SY5Y	brain:	n/a	n/a
7	JUND	chr3:42370172-42370290	HepG2	liver:	n/a	n/a
8	KAP1	chr3:42358554-42359075	HEK293	kidney:	n/a	n/a
9	KAP1	chr3:42355931-42356300	HEK293	kidney:	n/a	n/a
10	KAP1	chr3:42358461-42359291	K562	blood:	n/a	n/a
11	KAP1	chr3:42358630-42359090	U2OS	brain:	n/a	n/a
12	KAP1	chr3:42355954-42356212	U2OS	brain:	n/a	n/a
13	MAFK	chr3:42371536-42371579	HepG2	liver:	n/a	n/a
14	MAFK	chr3:42358978-42359225	HepG2	liver:	n/a	n/a
15	MAFK	chr3:42371048-42371198	HepG2	liver:	n/a	n/a
16	MYC	chr3:42371887-42372084	MCF10A-Er-Src	breast:	n/a	n/a
17	MYC	chr3:42362964-42363036	MCF-7	breast:	n/a	n/a
18	POLR2A	chr3:42362951-42363023	A549	lung:	n/a	n/a
19	POLR2A	chr3:42363010-42363064	MCF-7	breast:	n/a	n/a
20	POLR2A	chr3:42363001-42363005	MCF-7	breast:	n/a	n/a
21	POLR2A	chr3:42362916-42362946	A549	lung:	n/a	n/a
22	POLR2A	chr3:42356880-42356929	Gliobla	brain:	n/a	n/a
23	POLR2A	chr3:42368249-42368403	MCF10A-Er-Src	breast:	n/a	n/a
24	SETDB1	chr3:42355588-42356452	U2OS	brain:	n/a	n/a
25	SETDB1	chr3:42358378-42359137	U2OS	brain:	n/a	n/a
26	STAT3	chr3:42360560-42360615	MCF10A-Er-Src	breast:	n/a	n/a
27	STAT3	chr3:42367772-42367972	MCF10A-Er-Src	breast:	n/a	n/a
28	ZNF143	chr3:42355958-42356272	H1-hESC	embryonic stem cell:	n/a	n/a
29	ZNF143	chr3:42358903-42358910	H1-hESC	embryonic stem cell:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:42355817..42358731-chr3:42372025..42373776,2	MCF-7	breast:
2	chr3:42355817..42358731-chr3:42372025..42373776,2	MCF-7	breast:

No data

Variant related genes	Relation type
SALL4P6	TF binding region

Extended variants
information (count: 212 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:212 , 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	rs532041433	chr3:42358474-42358475	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs367620210	chr3:42358525-42358526	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs548448021	chr3:42358547-42358548	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs568338831	chr3:42358548-42358549	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs499475	chr3:42358549-42358550	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs146196884	chr3:42358571-42358572	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs566873253	chr3:42358591-42358592	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs61382037	chr3:42358619-42358620	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs74598574	chr3:42358627-42358628	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs539096539	chr3:42358646-42358647	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs374868470	chr3:42358653-42358654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs556417020	chr3:42358680-42358681	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs55985430	chr3:42358685-42358686	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs570556953	chr3:42358703-42358704	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs77818116	chr3:42358736-42358737	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs535741417	chr3:42358752-42358753	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs185538517	chr3:42358754-42358755	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551868429	chr3:42358795-42358796	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs556158919	chr3:42358817-42358818	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs530293568	chr3:42358844-42358845	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs78833727	chr3:42358883-42358884	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs188259327	chr3:42358925-42358926	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs560594779	chr3:42358937-42358938	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs577306374	chr3:42358945-42358946	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs545917310	chr3:42358950-42358951	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs562903913	chr3:42359086-42359087	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs199584823	chr3:42359153-42359154	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs149107455	chr3:42359170-42359171	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs534490708	chr3:42359281-42359282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs552881238	chr3:42360573-42360574	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs7634057	chr3:42360590-42360591	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs578148570	chr3:42360631-42360632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543127716	chr3:42360645-42360646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562234529	chr3:42360731-42360732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375374071	chr3:42360749-42360750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141526572	chr3:42360803-42360804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528872975	chr3:42360834-42360835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548958180	chr3:42360864-42360865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs474470	chr3:42360871-42360872	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs142877475	chr3:42360935-42360936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550308703	chr3:42360944-42360945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571334100	chr3:42361020-42361021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186825608	chr3:42361042-42361043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549999529	chr3:42361056-42361057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs151051418	chr3:42361076-42361077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191554348	chr3:42361132-42361133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555311207	chr3:42361199-42361200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs678574	chr3:42362817-42362818	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs550255404	chr3:42362860-42362861	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559919175	chr3:42362866-42362867	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Wilms tumour	17204608	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Kartagener syndrome	16639409	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:42360600-42361200	Enhancers	Brain Germinal Matrix	brain
2	chr3:42362800-42363600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:42362800-42363600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr3:42363200-42366600	Weak transcription	Right Atrium	heart
5	chr3:42369400-42369600	Bivalent Enhancer	HSMMtube	muscle
6	chr3:42369400-42369800	Enhancers	Colon Smooth Muscle	Colon

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