Variant report

Variant	nsv590278
Chromosome Location	chr3:51724147-51736744
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:36)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:36 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:51724676-51724803	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr3:51724760-51724910	HUVEC	blood vessel:	n/a	n/a
3	CTCF	chr3:51724699-51724831	HepG2	liver:	n/a	n/a
4	CTCF	chr3:51724660-51724810	HEK293	kidney:	n/a	n/a
5	CTCF	chr3:51724677-51724904	H1-hESC	embryonic stem cell:	n/a	n/a
6	GATA3	chr3:51726555-51726776	T-47D	breast:	n/a	n/a
7	MAZ	chr3:51725563-51725571	Hela-S3	cervix:	n/a	n/a
8	MYC	chr3:51729671-51729819	MCF-7	breast:	n/a	n/a
9	POLR2A	chr3:51734868-51734988	MCF-7	breast:	n/a	n/a
10	POLR2A	chr3:51730325-51730334	HepG2	liver:	n/a	n/a
11	POLR2A	chr3:51729459-51729480	GM12878	blood:	n/a	n/a
12	POLR2A	chr3:51727134-51727179	MCF-7	breast:	n/a	n/a
13	POLR2A	chr3:51730317-51730324	MCF-7	breast:	n/a	n/a
14	POLR2A	chr3:51734971-51735028	MCF-7	breast:	n/a	n/a
15	POLR2A	chr3:51730290-51730315	MCF-7	breast:	n/a	n/a
16	POLR2A	chr3:51730911-51731299	H1-neurons	neurons:	n/a	n/a
17	POLR2A	chr3:51730326-51730339	MCF-7	breast:	n/a	n/a
18	POLR2A	chr3:51729434-51729438	GM12878	blood:	n/a	n/a
19	POLR2A	chr3:51735031-51735048	MCF-7	breast:	n/a	n/a
20	POLR2A	chr3:51736499-51736667	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr3:51730369-51730409	HepG2	liver:	n/a	n/a
22	POLR2A	chr3:51727815-51728254	SK-N-MC	brain:	n/a	n/a
23	POLR2A	chr3:51729725-51729806	MCF-7	breast:	n/a	n/a
24	POLR2A	chr3:51729109-51729214	MCF-7	breast:	n/a	n/a
25	POLR2A	chr3:51736587-51736782	MCF-7	breast:	n/a	n/a
26	POLR2A	chr3:51730197-51730391	GM12878	blood:	n/a	n/a
27	POLR2A	chr3:51729586-51729599	GM12878	blood:	n/a	n/a
28	POLR2A	chr3:51732865-51732870	GM12878	blood:	n/a	n/a
29	POLR2A	chr3:51730921-51731319	H1-neurons	neurons:	n/a	n/a
30	POLR2A	chr3:51730221-51730271	MCF-7	breast:	n/a	n/a
31	RAD21	chr3:51724664-51724970	H1-hESC	embryonic stem cell:	n/a	n/a
32	RCOR1	chr3:51730945-51731326	K562	blood:	n/a	n/a
33	RCOR1	chr3:51731055-51731292	K562	blood:	n/a	n/a
34	REST	chr3:51730658-51731637	H1-neurons	neurons:	n/a	chr3:51731442-51731451 chr3:51731277-51731287
35	WRNIP1	chr3:51732061-51732074	GM12878	blood:	n/a	n/a
36	ZNF143	chr3:51724663-51724974	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:51725919-51725969	Jurkat	blood:	n/a
2	chr3:51725919-51725969	AG09309	skin:	n/a
3	chr3:51725919-51725969	GM12878	blood:	n/a
4	chr3:51725919-51725969	GM12891	blood:	n/a
5	chr3:51725919-51725969	AG04449	skin:	fetal
6	chr3:51725919-51725969	Hepatocyte	liver:	n/a
7	chr3:51725919-51725969	LNCaP	prostate:	n/a
8	chr3:51725919-51725969	U87	brain:	n/a
9	chr3:51725919-51725969	MCF10A-Er-Src	breast:	n/a
10	chr3:51725919-51725969	AG09319	gingival:	n/a
11	chr3:51725919-51725969	CMK	blood:	n/a
12	chr3:51725919-51725969	BJ	skin:	n/a
13	chr3:51725919-51725969	HIPEpiC	eye:	n/a
14	chr3:51725919-51725969	HNPCEpiC	eye:	n/a
15	chr3:51725919-51725969	T-47D	breast:	n/a
16	chr3:51725919-51725969	H1-hESC	embryonic stem cell:	embryo
17	chr3:51725919-51725969	PrEC	prostate:	n/a
18	chr3:51725919-51725969	MCF-7	breast:	n/a
19	chr3:51725919-51725969	ProgFib	skin:	n/a
20	chr3:51725919-51725969	HL-60	blood:	n/a
21	chr3:51725919-51725969	GM06990	blood:	n/a
22	chr3:51725919-51725969	HRCEpiC	kidney:	n/a
23	chr3:51725919-51725969	RPTEC	kidney:	n/a
24	chr3:51725919-51725969	SK-N-SH	brain:	n/a
25	chr3:51725919-51725969	HepG2	liver:	n/a
26	chr3:51725919-51725969	A549	lung:	n/a
27	chr3:51725919-51725969	HEK293	kidney:	embryo
28	chr3:51725919-51725969	NHBE	bronchial:	n/a
29	chr3:51725919-51725969	BE2_C	brain:	n/a
30	chr3:51725919-51725969	HCM	heart:	n/a
31	chr3:51725919-51725969	SKMC	muscle:	n/a
32	chr3:51725919-51725969	SAEC	small airway:	n/a
33	chr3:51725919-51725969	SK-N-SH_RA	brain:	n/a
34	chr3:51725919-51725969	HAEpiC	amniotic membrane:	n/a
35	chr3:51725919-51725969	NB4	blood:	n/a
36	chr3:51725919-51725969	HCT-116	colon:	n/a
37	chr3:51725919-51725969	GM12892	blood:	n/a
38	chr3:51725919-51725969	ovcar-3	ovarian:	n/a
39	chr3:51725919-51725969	AoSMC	blood vessel:	n/a
40	chr3:51725919-51725969	AG04450	lung:	fetal
41	chr3:51725919-51725969	HUVEC	blood vessel:	n/a
42	chr3:51725919-51725969	HMEC	breast:	n/a
43	chr3:51725919-51725969	Hela-S3	cervix:	n/a
44	chr3:51725919-51725969	NT2-D1	testis:	n/a
45	chr3:51725919-51725969	NHDF-neo	bronchial:	n/a
46	chr3:51725919-51725969	ECC-1	luminal epithelium:	n/a
47	chr3:51725919-51725969	PFSK-1	brain:	n/a
48	chr3:51725919-51725969	K562	blood:	n/a
49	chr3:51725919-51725969	HEEpiC	esophagus:	n/a
50	chr3:51725919-51725969	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:51734961..51737149-chr3:51738002..51740092,2	K562	blood:
2	chr3:51464596..51467000-chr3:51736520..51738058,2	MCF-7	breast:
3	chr3:51734229..51736388-chr3:51834430..51837314,2	K562	blood:
4	chr3:51729309..51731810-chr3:51740134..51741778,2	MCF-7	breast:
5	chr3:51727445..51729583-chr3:51732971..51735394,3	MCF-7	breast:

No data

Variant related genes	Relation type
RNA5SP132	TF binding region
GRM2	TF binding region
RNA5SP132	CpG island
GRM2	CpG island
ENSG00000164082	chromatin interactions
ENSG00000201595	chromatin interactions

Extended variants
information (count: 391 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9880050	chr3:51724147-51724148	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186502794	chr3:51724152-51724153	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538881667	chr3:51724200-51724201	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143501748	chr3:51724206-51724207	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376741392	chr3:51724298-51724299	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540187763	chr3:51724321-51724322	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561946656	chr3:51724358-51724359	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573844299	chr3:51724374-51724375	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544209299	chr3:51724439-51724440	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377082359	chr3:51724462-51724463	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188095259	chr3:51724512-51724513	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370858602	chr3:51724543-51724544	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111939174	chr3:51724568-51724569	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557183438	chr3:51724630-51724631	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142166323	chr3:51724689-51724690	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs36098912	chr3:51724760-51724761	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375203681	chr3:51724762-51724763	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560262369	chr3:51724784-51724785	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575439819	chr3:51724877-51724878	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560245988	chr3:51724906-51724907	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536376631	chr3:51725041-51725042	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527394698	chr3:51725047-51725048	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550646198	chr3:51725119-51725120	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35862344	chr3:51725137-51725138	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529351650	chr3:51725141-51725142	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548930636	chr3:51725142-51725143	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567170666	chr3:51725177-51725178	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536122350	chr3:51725221-51725222	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs180929001	chr3:51725229-51725230	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186106621	chr3:51725287-51725288	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201830075	chr3:51725454-51725455	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115236540	chr3:51725456-51725457	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557931833	chr3:51725464-51725465	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112039725	chr3:51725507-51725508	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115400355	chr3:51725534-51725535	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191398675	chr3:51725628-51725629	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549321287	chr3:51725727-51725728	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573986220	chr3:51725780-51725781	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544486725	chr3:51725912-51725913	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562687151	chr3:51725920-51725921	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147516982	chr3:51725933-51725934	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562759525	chr3:51725994-51725995	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545185931	chr3:51725995-51725996	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138532216	chr3:51726014-51726015	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540181264	chr3:51726015-51726016	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530805745	chr3:51726057-51726058	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548831020	chr3:51726096-51726097	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560922368	chr3:51726097-51726098	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs5848930	chr3:51726104-51726105	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377423704	chr3:51726124-51726125	Genic enhancers Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51706400-51733400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr3:51706400-51741000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr3:51706600-51724600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr3:51706600-51739600	Weak transcription	Small Intestine	intestine
5	chr3:51707800-51740400	Strong transcription	Fetal Intestine Small	intestine
6	chr3:51708800-51738800	Strong transcription	Fetal Intestine Large	intestine
7	chr3:51716200-51726200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr3:51716200-51737000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr3:51716400-51741200	Weak transcription	Fetal Kidney	kidney
10	chr3:51716600-51724800	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr3:51716800-51726600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr3:51716800-51738800	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr3:51717000-51727400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr3:51717400-51739800	Strong transcription	Liver	Liver
15	chr3:51717800-51725200	Strong transcription	Gastric	stomach
16	chr3:51718000-51726800	Strong transcription	Pancreas	Pancrea
17	chr3:51719600-51726000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:51719600-51741200	Weak transcription	NHDF-Ad	bronchial
19	chr3:51719800-51732400	Weak transcription	Hela-S3	cervix
20	chr3:51720000-51733200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr3:51720200-51733000	Weak transcription	Fetal Lung	lung
22	chr3:51720400-51727200	Strong transcription	Duodenum Smooth Muscle	Duodenum
23	chr3:51720600-51739800	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr3:51720600-51740000	Strong transcription	Sigmoid Colon	Sigmoid Colon
25	chr3:51721000-51724600	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr3:51721000-51735600	Weak transcription	K562	blood
27	chr3:51721000-51738200	Weak transcription	A549	lung
28	chr3:51721000-51741000	Weak transcription	HUVEC	blood vessel
29	chr3:51721200-51724200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr3:51721200-51724200	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr3:51721200-51724200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr3:51721200-51724400	Strong transcription	Brain Hippocampus Middle	brain
33	chr3:51721400-51724400	Strong transcription	GM12878-XiMat	blood
34	chr3:51721400-51734200	Genic enhancers	Primary T cells fromperipheralblood	blood
35	chr3:51721400-51738800	Strong transcription	Colonic Mucosa	Colon
36	chr3:51721400-51739400	Strong transcription	Thymus	Thymus
37	chr3:51721400-51739800	Strong transcription	Duodenum Mucosa	Duodenum
38	chr3:51721400-51740000	Strong transcription	Placenta	Placenta
39	chr3:51721400-51740200	Strong transcription	Esophagus	oesophagus
40	chr3:51721400-51740400	Strong transcription	Dnd41	blood
41	chr3:51721400-51740600	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr3:51721400-51740800	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr3:51721600-51724200	Strong transcription	Brain Anterior Caudate	brain
44	chr3:51721600-51725000	Strong transcription	Lung	lung
45	chr3:51721600-51725200	Weak transcription	Fetal Brain Female	brain
46	chr3:51721600-51725400	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
47	chr3:51721600-51726200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr3:51721600-51727600	Strong transcription	Ovary	ovary
49	chr3:51721600-51739400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr3:51721600-51740400	Strong transcription	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links