Variant report

Variant	esv3474024
Chromosome Location	chr6:58186793-58190915
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	FOSL2	chr6:58186839-58187252	HepG2	liver:	n/a	n/a
2	FOSL2	chr6:58187380-58187723	HepG2	liver:	n/a	n/a
3	FOXA1	chr6:58186888-58187339	HepG2	liver:	n/a	n/a
4	JUND	chr6:58186975-58187151	HepG2	liver:	n/a	n/a
5	PAX5	chr6:58187510-58187697	GM12878	blood:	n/a	n/a
6	USF1	chr6:58186990-58187124	HepG2	liver:	n/a	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAG2-4	chr6:58186873-58187271	XLOC_005332
2	lnc-RAB23-17	chr6:58186881-58187205	NONHSAT113305

Variant related genes	Relation type
ENSG00000272541	TF binding region

Extended variants
information (count: 34 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562209685	chr6:58186844-58186845	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs114461005	chr6:58186855-58186856	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs541974028	chr6:58186862-58186863	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563164282	chr6:58186893-58186894	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs371267561	chr6:58186904-58186905	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs142192287	chr6:58186959-58186960	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs2758387	chr6:58186967-58186968	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs545700713	chr6:58186997-58186998	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs563727855	chr6:58187017-58187018	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs150730782	chr6:58187055-58187056	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs546354330	chr6:58187114-58187115	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs551027446	chr6:58187187-58187188	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs528997084	chr6:58187215-58187216	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs9391420	chr6:58187267-58187268	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs2258186	chr6:58187282-58187283	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
16	rs540098486	chr6:58187305-58187306	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs558529566	chr6:58187325-58187326	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs2258185	chr6:58187327-58187328	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
19	rs555492617	chr6:58187396-58187397	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs574050227	chr6:58187413-58187414	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs537954779	chr6:58187426-58187427	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs186680477	chr6:58187460-58187461	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs545686684	chr6:58187476-58187477	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs4087121	chr6:58187492-58187493	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs369284878	chr6:58187505-58187506	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs546885354	chr6:58187506-58187507	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs572737140	chr6:58187507-58187508	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs540193602	chr6:58187515-58187516	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs561553795	chr6:58187637-58187638	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs528938404	chr6:58187650-58187651	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs191982275	chr6:58187697-58187698	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs563063957	chr6:58187713-58187714	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs533614289	chr6:58187714-58187715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs144413484	chr6:58187715-58187716	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:0 , 50 per page) page:

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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