Variant report

Variant	esv3410055
Chromosome Location	chr3:51737012-51741510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:232)
CpG islands
(count:610)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:232 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:51740735-51741003	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:51740809-51741013	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr3:51740768-51740996	K562	blood:	n/a	n/a
4	CEBPD	chr3:51740798-51740998	HepG2	liver:	n/a	n/a
5	CHD2	chr3:51740871-51740973	HepG2	liver:	n/a	n/a
6	CHD2	chr3:51740767-51741059	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr3:51737580-51737695	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr3:51740786-51741151	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr3:51740860-51741010	HMF	breast:	n/a	n/a
10	CTCF	chr3:51740820-51740970	HAc	cerebellar:	n/a	n/a
11	CTCF	chr3:51740840-51740990	HPF	lung:	n/a	n/a
12	CTCF	chr3:51740820-51740970	HEK293	kidney:	n/a	n/a
13	CTCF	chr3:51740840-51740990	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr3:51740840-51740990	HCFaa	heart:	n/a	n/a
15	CTCF	chr3:51740840-51740990	AG04449	skin:	n/a	n/a
16	CTCF	chr3:51740849-51740970	Pancreas_OC	pancreas:	n/a	n/a
17	CTCF	chr3:51740820-51740970	Caco-2	colon:	n/a	n/a
18	CTCF	chr3:51740860-51741010	BJ	skin:	n/a	n/a
19	CTCF	chr3:51740880-51741030	HVMF	connective:	n/a	n/a
20	CTCF	chr3:51740893-51740958	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr3:51740860-51741010	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr3:51740801-51740984	IMR90	lung:	n/a	n/a
23	CTCF	chr3:51740820-51740970	AG04450	lung:	n/a	n/a
24	CTCF	chr3:51740911-51740966	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr3:51740800-51740950	HA-sp	spinal cord:	n/a	n/a
26	CTCF	chr3:51740820-51740970	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr3:51740860-51741010	HMEC	breast:	n/a	n/a
28	CTCF	chr3:51740800-51740950	BJ	skin:	n/a	n/a
29	CTCF	chr3:51740840-51740990	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr3:51740820-51740970	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr3:51740840-51740990	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr3:51740840-51740990	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr3:51740840-51740990	SAEC	small airway:	n/a	n/a
34	CTCF	chr3:51740820-51740970	AG09319	gingival:	n/a	n/a
35	CTCF	chr3:51740840-51740990	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr3:51740840-51740990	HCPEpiC	choroid plexus:	n/a	n/a
37	E2F6	chr3:51740850-51741682	H1-hESC	embryonic stem cell:	n/a	n/a
38	E2F6	chr3:51740935-51741594	H1-hESC	embryonic stem cell:	n/a	n/a
39	EGR1	chr3:51740823-51740988	K562	blood:	n/a	n/a
40	EGR1	chr3:51740815-51741002	K562	blood:	n/a	n/a
41	EGR1	chr3:51737358-51737694	H1-hESC	embryonic stem cell:	n/a	n/a
42	ELF1	chr3:51741295-51741706	GM12878	blood:	n/a	n/a
43	EP300	chr3:51740767-51740996	H1-hESC	embryonic stem cell:	n/a	n/a
44	EP300	chr3:51740650-51741266	ECC-1	luminal epithelium:	n/a	n/a
45	ETS1	chr3:51740787-51740988	K562	blood:	n/a	n/a
46	FOXP2	chr3:51740810-51741008	PFSK-1	brain:	n/a	n/a
47	GABPA	chr3:51741042-51741448	H1-hESC	embryonic stem cell:	n/a	chr3:51741075-51741084
48	GABPA	chr3:51740784-51740990	H1-hESC	embryonic stem cell:	n/a	n/a
49	GTF2F1	chr3:51740818-51740951	H1-hESC	embryonic stem cell:	n/a	n/a
50	GTF2F1	chr3:51741223-51741301	H1-hESC	embryonic stem cell:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:51740896-51740946	ovcar-3	ovarian:	n/a
2	chr3:51740896-51740946	PrEC	prostate:	n/a
3	chr3:51740896-51740946	HCT-116	colon:	n/a
4	chr3:51739481-51739531	GM12892	blood:	n/a
5	chr3:51739481-51739531	HRCEpiC	kidney:	n/a
6	chr3:51741473-51741523	Jurkat	blood:	n/a
7	chr3:51741135-51741185	PFSK-1	brain:	n/a
8	chr3:51741473-51741523	RPTEC	kidney:	n/a
9	chr3:51740896-51740946	BE2_C	brain:	n/a
10	chr3:51741473-51741523	T-47D	breast:	n/a
11	chr3:51737930-51737980	HNPCEpiC	eye:	n/a
12	chr3:51740896-51740946	NHDF-neo	bronchial:	n/a
13	chr3:51741473-51741523	PFSK-1	brain:	n/a
14	chr3:51741473-51741523	PANC-1	pancreas:	n/a
15	chr3:51740741-51740791	BE2_C	brain:	n/a
16	chr3:51741135-51741185	GM12892	blood:	n/a
17	chr3:51739481-51739531	NB4	blood:	n/a
18	chr3:51740201-51740251	ProgFib	skin:	n/a
19	chr3:51737930-51737980	AG09319	gingival:	n/a
20	chr3:51740741-51740791	H1-hESC	embryonic stem cell:	embryo
21	chr3:51740201-51740251	HRE	kidney:	n/a
22	chr3:51740850-51740900	H1-hESC	embryonic stem cell:	embryo
23	chr3:51741473-51741523	SK-N-MC	brain:	n/a
24	chr3:51740201-51740251	HEEpiC	esophagus:	n/a
25	chr3:51740741-51740791	HRE	kidney:	n/a
26	chr3:51740741-51740791	AG10803	skin:	n/a
27	chr3:51741135-51741185	ovcar-3	ovarian:	n/a
28	chr3:51740875-51740925	SK-N-SH_RA	brain:	n/a
29	chr3:51741135-51741185	SK-N-SH	brain:	n/a
30	chr3:51741473-51741523	GM12892	blood:	n/a
31	chr3:51740875-51740925	Jurkat	blood:	n/a
32	chr3:51737930-51737980	PANC-1	pancreas:	n/a
33	chr3:51741280-51741330	HL-60	blood:	n/a
34	chr3:51740850-51740900	HNPCEpiC	eye:	n/a
35	chr3:51739481-51739531	AG04450	lung:	fetal
36	chr3:51740875-51740925	GM12891	blood:	n/a
37	chr3:51740896-51740946	HCPEpiC	choroid plexus:	n/a
38	chr3:51740850-51740900	K562	blood:	n/a
39	chr3:51740896-51740946	SKMC	muscle:	n/a
40	chr3:51737930-51737980	HEEpiC	esophagus:	n/a
41	chr3:51740741-51740791	Hepatocyte	liver:	n/a
42	chr3:51740850-51740900	AG04450	lung:	fetal
43	chr3:51741280-51741330	HNPCEpiC	eye:	n/a
44	chr3:51741473-51741523	MCF-7	breast:	n/a
45	chr3:51739481-51739531	SK-N-SH	brain:	n/a
46	chr3:51740850-51740900	HCF	heart:	n/a
47	chr3:51740741-51740791	NHBE	bronchial:	n/a
48	chr3:51739481-51739531	HEEpiC	esophagus:	n/a
49	chr3:51740850-51740900	HUVEC	blood vessel:	n/a
50	chr3:51741473-51741523	H1-hESC	embryonic stem cell:	embryo

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:51464596..51467000-chr3:51736520..51738058,2	MCF-7	breast:
2	chr3:51739711..51741988-chr3:51976226..51978640,2	K562	blood:
3	chr3:51734961..51737149-chr3:51738002..51740092,2	K562	blood:
4	chr3:51726622..51728769-chr3:51737176..51738724,2	MCF-7	breast:
5	chr3:51734961..51737149-chr3:51738002..51740092,2	K562	blood:

No data

Variant related genes	Relation type
GRM2	TF binding region
GRM2	CpG island
ENSG00000041880	chromatin interactions
ENSG00000201595	chromatin interactions

Extended variants
information (count: 161 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:161 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576813754	chr3:51737027-51737028	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs139193626	chr3:51737103-51737104	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554401010	chr3:51737138-51737139	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187737896	chr3:51737139-51737140	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373646707	chr3:51737166-51737167	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377016564	chr3:51737196-51737197	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs145322604	chr3:51737229-51737230	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs386660898	chr3:51737237-51737238	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531814682	chr3:51737239-51737240	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543965240	chr3:51737243-51737244	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565268485	chr3:51737339-51737340	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs72953429	chr3:51737355-51737356	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs190862716	chr3:51737510-51737511	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs565924412	chr3:51737518-51737519	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs112362203	chr3:51737537-51737538	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs376166417	chr3:51737538-51737539	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs372591392	chr3:51737540-51737541	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs529960909	chr3:51737546-51737547	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs547953091	chr3:51737548-51737549	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs569549400	chr3:51737596-51737597	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs536740560	chr3:51737656-51737657	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs147550471	chr3:51737663-51737664	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs199688268	chr3:51737702-51737703	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs534571964	chr3:51737715-51737716	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs548042685	chr3:51737730-51737731	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs370467260	chr3:51737761-51737762	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs374502236	chr3:51737785-51737786	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371661771	chr3:51737795-51737796	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs375133563	chr3:51737824-51737825	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs369579500	chr3:51737839-51737840	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs200027537	chr3:51737846-51737847	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs28994878	chr3:51737852-51737853	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs200798093	chr3:51737853-51737854	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs371693880	chr3:51737861-51737862	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs375977287	chr3:51737866-51737867	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs369013696	chr3:51737867-51737868	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs555183400	chr3:51737882-51737883	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs367741404	chr3:51737908-51737909	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs11553574	chr3:51737965-51737966	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs61737032	chr3:51737995-51737996	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs565332036	chr3:51738013-51738014	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs550338628	chr3:51738016-51738017	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs532507096	chr3:51738027-51738028	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs182500036	chr3:51738046-51738047	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs559509307	chr3:51738050-51738051	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs529986462	chr3:51738077-51738078	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs12141	chr3:51738089-51738090	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs2518461	chr3:51738101-51738102	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs536124226	chr3:51738122-51738123	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs187198574	chr3:51738153-51738154	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Pancreatic endocrine tumor	17639061	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51706400-51741000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr3:51706600-51739600	Weak transcription	Small Intestine	intestine
3	chr3:51707800-51740400	Strong transcription	Fetal Intestine Small	intestine
4	chr3:51708800-51738800	Strong transcription	Fetal Intestine Large	intestine
5	chr3:51716400-51741200	Weak transcription	Fetal Kidney	kidney
6	chr3:51716800-51738800	Strong transcription	Cortex derived primary cultured neurospheres	brain
7	chr3:51717400-51739800	Strong transcription	Liver	Liver
8	chr3:51719600-51741200	Weak transcription	NHDF-Ad	bronchial
9	chr3:51720600-51739800	Strong transcription	Rectal Mucosa Donor 29	rectum
10	chr3:51720600-51740000	Strong transcription	Sigmoid Colon	Sigmoid Colon
11	chr3:51721000-51738200	Weak transcription	A549	lung
12	chr3:51721000-51741000	Weak transcription	HUVEC	blood vessel
13	chr3:51721400-51738800	Strong transcription	Colonic Mucosa	Colon
14	chr3:51721400-51739400	Strong transcription	Thymus	Thymus
15	chr3:51721400-51739800	Strong transcription	Duodenum Mucosa	Duodenum
16	chr3:51721400-51740000	Strong transcription	Placenta	Placenta
17	chr3:51721400-51740200	Strong transcription	Esophagus	oesophagus
18	chr3:51721400-51740400	Strong transcription	Dnd41	blood
19	chr3:51721400-51740600	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr3:51721400-51740800	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr3:51721600-51739400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr3:51721600-51740400	Strong transcription	Fetal Stomach	stomach
23	chr3:51721600-51740800	Weak transcription	HSMM	muscle
24	chr3:51721800-51740200	Strong transcription	Stomach Smooth Muscle	stomach
25	chr3:51722200-51739200	Strong transcription	Fetal Muscle Leg	muscle
26	chr3:51722400-51739000	Strong transcription	Fetal Muscle Trunk	muscle
27	chr3:51722400-51740200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr3:51722600-51740000	Strong transcription	Primary B cells from peripheral blood	blood
29	chr3:51722600-51741200	Weak transcription	Stomach Mucosa	stomach
30	chr3:51723200-51738600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr3:51723800-51738200	Strong transcription	Fetal Thymus	thymus
32	chr3:51723800-51739400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr3:51724000-51739000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr3:51724000-51740200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr3:51724000-51740400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:51724400-51741200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr3:51725400-51740800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr3:51725600-51740000	Strong transcription	Lung	lung
39	chr3:51725600-51740200	Strong transcription	Gastric	stomach
40	chr3:51726200-51738800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr3:51726400-51737200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:51727000-51739200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:51727400-51740200	Weak transcription	Psoas Muscle	Psoas
44	chr3:51728000-51739600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr3:51728200-51738800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr3:51728200-51740200	Strong transcription	Adipose Nuclei	Adipose
47	chr3:51728400-51739400	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr3:51728400-51740000	Strong transcription	Aorta	Aorta
49	chr3:51728800-51740000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr3:51729000-51739400	Strong transcription	Brain Hippocampus Middle	brain

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