Variant report

Variant	nsv979833
Chromosome Location	chr3:52387550-52407592
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:112)
CpG islands
(count:244)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:112 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr3:52407210-52407430	K562	blood:	n/a	chr3:52407221-52407230
2	CHD2	chr3:52407264-52407271	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr3:52407280-52407430	GM12869	blood:	n/a	n/a
4	CTCF	chr3:52407319-52407332	GM13976	blood:	n/a	n/a
5	CTCF	chr3:52407240-52407390	GM12871	blood:	n/a	n/a
6	CTCF	chr3:52407151-52407416	K562	blood:	n/a	n/a
7	CTCF	chr3:52407279-52407346	GM12878	blood:	n/a	n/a
8	CTCF	chr3:52407280-52407430	GM12873	blood:	n/a	n/a
9	CTCF	chr3:52407220-52407370	GM12875	blood:	n/a	n/a
10	CTCF	chr3:52407242-52407411	GM12892	blood:	n/a	n/a
11	CTCF	chr3:52407310-52407319	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr3:52407296-52407390	Lung_OC	lung:	n/a	n/a
13	CTCF	chr3:52407240-52407390	GM12866	blood:	n/a	n/a
14	CTCF	chr3:52407258-52407409	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr3:52407299-52407327	GM12878	blood:	n/a	n/a
16	CTCF	chr3:52407253-52407392	GM10248	blood:	n/a	n/a
17	CTCF	chr3:52407228-52407432	GM12891	blood:	n/a	n/a
18	CTCF	chr3:52399680-52399830	HepG2	liver:	n/a	n/a
19	CTCF	chr3:52407260-52407410	GM12874	blood:	n/a	n/a
20	CTCF	chr3:52407160-52407310	SAEC	small airway:	n/a	n/a
21	CTCF	chr3:52407140-52407290	GM06990	blood:	n/a	n/a
22	CTCF	chr3:52407280-52407430	GM12867	blood:	n/a	n/a
23	CTCF	chr3:52407270-52407379	GM19240	blood:	n/a	n/a
24	CTCF	chr3:52407234-52407428	GM19238	blood:	n/a	n/a
25	CTCF	chr3:52407161-52407501	K562	blood:	n/a	n/a
26	CTCF	chr3:52407247-52407307	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr3:52407252-52407441	GM19239	blood:	n/a	n/a
28	CTCF	chr3:52407248-52407424	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr3:52407149-52407481	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr3:52407135-52407456	K562	blood:	n/a	n/a
31	CTCF	chr3:52407220-52407370	GM12871	blood:	n/a	n/a
32	CTCF	chr3:52407220-52407370	K562	blood:	n/a	n/a
33	CTCF	chr3:52407221-52407442	K562	blood:	n/a	n/a
34	CTCF	chr3:52407136-52407415	K562	blood:	n/a	n/a
35	CTCF	chr3:52399648-52399731	H1-hESC	embryonic stem cell:	n/a	chr3:52399676-52399694 chr3:52399659-52399667
36	E2F6	chr3:52407269-52407396	K562	blood:	n/a	n/a
37	E2F6	chr3:52407223-52407422	K562	blood:	n/a	n/a
38	EBF1	chr3:52407213-52407436	GM12878	blood:	n/a	n/a
39	EGR1	chr3:52407215-52407470	GM12878	blood:	n/a	n/a
40	EGR1	chr3:52407105-52407538	K562	blood:	n/a	n/a
41	EGR1	chr3:52407126-52407516	K562	blood:	n/a	n/a
42	EGR1	chr3:52390245-52390391	K562	blood:	n/a	chr3:52390335-52390346 chr3:52390371-52390381 chr3:52390335-52390346 chr3:52390334-52390348 chr3:52390337-52390346
43	EGR1	chr3:52407179-52407451	GM12878	blood:	n/a	n/a
44	ELF1	chr3:52407153-52407447	K562	blood:	n/a	chr3:52407241-52407253 chr3:52407239-52407248
45	ELF1	chr3:52406762-52407468	GM12878	blood:	n/a	chr3:52407241-52407253 chr3:52407239-52407248
46	ELF1	chr3:52407226-52407429	K562	blood:	n/a	chr3:52407241-52407253 chr3:52407239-52407248
47	EP300	chr3:52407375-52407397	GM12878	blood:	n/a	n/a
48	EP300	chr3:52407297-52407409	GM12878	blood:	n/a	n/a
49	HCFC1	chr3:52407270-52407342	K562	blood:	n/a	n/a
50	HMGN3	chr3:52407251-52407480	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:52407344-52407394	HRPEpiC	eye:	n/a
2	chr3:52393309-52393359	CMK	blood:	n/a
3	chr3:52407344-52407394	HL-60	blood:	n/a
4	chr3:52407081-52407131	HRPEpiC	eye:	n/a
5	chr3:52407081-52407131	SK-N-MC	brain:	n/a
6	chr3:52407081-52407131	U87	brain:	n/a
7	chr3:52407344-52407394	MCF-7	breast:	n/a
8	chr3:52407402-52407452	IMR90	lung:	fetal
9	chr3:52407344-52407394	CMK	blood:	n/a
10	chr3:52407081-52407131	NB4	blood:	n/a
11	chr3:52407344-52407394	AG09309	skin:	n/a
12	chr3:52407402-52407452	Caco-2	colon:	n/a
13	chr3:52393309-52393359	SK-N-MC	brain:	n/a
14	chr3:52407402-52407452	MCF-7	breast:	n/a
15	chr3:52393309-52393359	HCM	heart:	n/a
16	chr3:52407081-52407131	BJ	skin:	n/a
17	chr3:52407344-52407394	K562	blood:	n/a
18	chr3:52407402-52407452	BJ	skin:	n/a
19	chr3:52407344-52407394	HEK293	kidney:	embryo
20	chr3:52393309-52393359	GM12878	blood:	n/a
21	chr3:52407402-52407452	T-47D	breast:	n/a
22	chr3:52407402-52407452	HRCEpiC	kidney:	n/a
23	chr3:52407344-52407394	SK-N-SH	brain:	n/a
24	chr3:52407081-52407131	SK-N-SH_RA	brain:	n/a
25	chr3:52407402-52407452	HRPEpiC	eye:	n/a
26	chr3:52393309-52393359	ProgFib	skin:	n/a
27	chr3:52407081-52407131	AG09309	skin:	n/a
28	chr3:52407402-52407452	Hela-S3	cervix:	n/a
29	chr3:52407344-52407394	HMEC	breast:	n/a
30	chr3:52407402-52407452	AG04450	lung:	fetal
31	chr3:52407402-52407452	PrEC	prostate:	n/a
32	chr3:52407344-52407394	HCF	heart:	n/a
33	chr3:52407344-52407394	SK-N-SH_RA	brain:	n/a
34	chr3:52407081-52407131	HUVEC	blood vessel:	n/a
35	chr3:52393309-52393359	Hela-S3	cervix:	n/a
36	chr3:52407344-52407394	AG09319	gingival:	n/a
37	chr3:52407081-52407131	AG04450	lung:	fetal
38	chr3:52407081-52407131	HCPEpiC	choroid plexus:	n/a
39	chr3:52407344-52407394	MCF10A-Er-Src	breast:	n/a
40	chr3:52407344-52407394	HepG2	liver:	n/a
41	chr3:52407081-52407131	PANC-1	pancreas:	n/a
42	chr3:52407402-52407452	SAEC	small airway:	n/a
43	chr3:52393309-52393359	NB4	blood:	n/a
44	chr3:52407344-52407394	SKMC	muscle:	n/a
45	chr3:52393309-52393359	AoSMC	blood vessel:	n/a
46	chr3:52407402-52407452	RPTEC	kidney:	n/a
47	chr3:52393309-52393359	HEK293	kidney:	embryo
48	chr3:52407344-52407394	IMR90	lung:	fetal
49	chr3:52407081-52407131	NT2-D1	testis:	n/a
50	chr3:52407081-52407131	PFSK-1	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:52399836..52402473-chr3:52409418..52411150,2	K562	blood:
2	chr3:52272390..52274822-chr3:52406008..52407949,2	K562	blood:
3	chr3:52272785..52274922-chr3:52398332..52400991,2	K562	blood:
4	chr3:52391704..52393563-chr3:52402367..52404938,2	MCF-7	breast:
5	chr3:52400970..52402826-chr3:52442987..52445575,2	K562	blood:
6	chr3:52321755..52323526-chr3:52405745..52408434,2	K562	blood:
7	chr3:52384981..52388271-chr3:52408939..52411277,3	K562	blood:
8	chr3:52401882..52403404-chr3:52567843..52570372,2	K562	blood:
9	chr3:52310461..52311969-chr3:52386050..52388691,2	K562	blood:
10	chr3:52389433..52392179-chr3:52403246..52405082,2	K562	blood:
11	chr3:52388262..52390856-chr3:52397247..52399479,2	K562	blood:
12	chr3:52399471..52401376-chr3:52402846..52405775,2	K562	blood:
13	chr3:52406156..52409184-chr3:52415561..52421026,5	K562	blood:
14	chr3:52393060..52394976-chr3:52400289..52402060,2	K562	blood:
15	chr3:52269274..52272214-chr3:52398381..52400803,2	K562	blood:
16	chr3:52399471..52401376-chr3:52402846..52405775,2	K562	blood:
17	chr3:52388262..52390856-chr3:52397247..52399479,2	K562	blood:
18	chr3:52406883..52409184-chr3:52415694..52419355,3	K562	blood:
19	chr3:52391704..52393563-chr3:52402367..52404938,2	MCF-7	breast:
20	chr3:52393007..52395595-chr3:52397371..52399366,2	K562	blood:
21	chr3:52018451..52021014-chr3:52404106..52407054,2	K562	blood:
22	chr3:52389433..52392179-chr3:52403246..52405082,2	K562	blood:
23	chr3:52393060..52394976-chr3:52400289..52402060,2	K562	blood:
24	chr3:52390322..52390942-chr3:52419226..52419756,2	MCF-7	breast:

No data

Variant related genes	Relation type
DNAH1	TF binding region
ENSG00000239557	TF binding region
DNAH1	CpG island
ENSG00000239557	CpG island
ENSG00000168268	chromatin interactions
ENSG00000163930	chromatin interactions
ENSG00000243224	chromatin interactions
ENSG00000239732	chromatin interactions
ENSG00000164091	chromatin interactions
ENSG00000168273	chromatin interactions
ENSG00000010318	chromatin interactions
ENSG00000168237	chromatin interactions
ENSG00000114841	chromatin interactions
ENSG00000247596	chromatin interactions
ENSG00000243989	chromatin interactions

Extended variants
information (count: 917 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367804335	chr3:52387559-52387560	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552076854	chr3:52387568-52387569	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371840562	chr3:52387596-52387597	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571987789	chr3:52387600-52387601	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534534857	chr3:52387601-52387602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs61734641	chr3:52387605-52387606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368850443	chr3:52387607-52387608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76983136	chr3:52387620-52387621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544674332	chr3:52387629-52387630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372168540	chr3:52387644-52387645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566501109	chr3:52387665-52387666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535160318	chr3:52387666-52387667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555047992	chr3:52387833-52387834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180942589	chr3:52387854-52387855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185456377	chr3:52387878-52387879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557565118	chr3:52387883-52387884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577494488	chr3:52387884-52387885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540567652	chr3:52387922-52387923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575190512	chr3:52387925-52387926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560277448	chr3:52387971-52387972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565061197	chr3:52388025-52388026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573988896	chr3:52388030-52388031	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542711957	chr3:52388061-52388062	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190215187	chr3:52388074-52388075	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115913696	chr3:52388081-52388082	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551990713	chr3:52388119-52388120	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183463292	chr3:52388125-52388126	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550734368	chr3:52388126-52388127	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544490707	chr3:52388148-52388149	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527967981	chr3:52388176-52388177	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548075800	chr3:52388237-52388238	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs137943611	chr3:52388289-52388290	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565610604	chr3:52388350-52388351	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535455171	chr3:52388351-52388352	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548632675	chr3:52388365-52388366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568595656	chr3:52388369-52388370	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527961908	chr3:52388372-52388373	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557527260	chr3:52388387-52388388	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111311240	chr3:52388388-52388389	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188197681	chr3:52388410-52388411	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533806257	chr3:52388542-52388543	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551410758	chr3:52388651-52388652	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142113677	chr3:52388660-52388661	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185887057	chr3:52388667-52388668	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373563155	chr3:52388722-52388723	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs71297393	chr3:52388727-52388728	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs556630454	chr3:52388745-52388746	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576606278	chr3:52388747-52388748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145104015	chr3:52388768-52388769	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545556556	chr3:52388784-52388785	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	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
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
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Lung cancer	16618734	CNVD
Neuroblastoma	19686582	CNVD
Renal cell carcinoma	18765545	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52364800-52394400	Weak transcription	HSMMtube	muscle
2	chr3:52373800-52396000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr3:52374000-52399000	Weak transcription	Stomach Mucosa	stomach
4	chr3:52374000-52407000	Strong transcription	Fetal Intestine Small	intestine
5	chr3:52374200-52427000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr3:52375400-52405600	Strong transcription	Lung	lung
7	chr3:52376400-52402000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr3:52377000-52406600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr3:52377000-52406600	Strong transcription	Liver	Liver
10	chr3:52377200-52390600	Strong transcription	Primary T cells from cord blood	blood
11	chr3:52377200-52405200	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr3:52377400-52397400	Strong transcription	Brain Inferior Temporal Lobe	brain
13	chr3:52377400-52404800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr3:52377400-52406600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr3:52377400-52406800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr3:52377600-52406200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr3:52377800-52406200	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr3:52377800-52407200	Strong transcription	Fetal Intestine Large	intestine
19	chr3:52378200-52391600	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr3:52378400-52400000	Strong transcription	Brain Anterior Caudate	brain
21	chr3:52378400-52401200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr3:52378400-52401200	Strong transcription	Gastric	stomach
23	chr3:52378400-52401800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr3:52378600-52389800	Strong transcription	Sigmoid Colon	Sigmoid Colon
25	chr3:52378600-52390800	Strong transcription	Thymus	Thymus
26	chr3:52378600-52400000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr3:52378600-52400200	Strong transcription	Brain Cingulate Gyrus	brain
28	chr3:52378600-52400200	Strong transcription	Brain Hippocampus Middle	brain
29	chr3:52378600-52405000	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr3:52378600-52406800	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr3:52379200-52389800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr3:52379200-52391000	Strong transcription	Primary B cells from cord blood	blood
33	chr3:52379400-52410600	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr3:52380400-52401000	Strong transcription	Placenta	Placenta
35	chr3:52380800-52396400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr3:52381400-52401200	Strong transcription	Ovary	ovary
37	chr3:52381400-52402600	Strong transcription	Fetal Stomach	stomach
38	chr3:52381400-52404200	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr3:52381400-52407400	Weak transcription	NHLF	lung
40	chr3:52381600-52392600	Weak transcription	Colon Smooth Muscle	Colon
41	chr3:52381600-52396400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr3:52381600-52397600	Strong transcription	Stomach Smooth Muscle	stomach
43	chr3:52381600-52405400	Strong transcription	Adipose Nuclei	Adipose
44	chr3:52381600-52405800	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chr3:52381800-52397000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr3:52382000-52389600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr3:52382000-52390000	Strong transcription	Right Ventricle	heart
48	chr3:52382200-52395800	Weak transcription	Psoas Muscle	Psoas
49	chr3:52382400-52396000	Strong transcription	Colonic Mucosa	Colon
50	chr3:52382600-52387600	Strong transcription	Primary hematopoietic stem cells	blood

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