Variant report

Variant	nsv584058
Chromosome Location	chr2:189799499-189855943
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	ATF1	chr2:189807452-189807586	K562	blood:	n/a	n/a
2	ATF2	chr2:189843359-189843871	GM12878	blood:	n/a	n/a
3	ATF2	chr2:189843358-189843943	GM12878	blood:	n/a	n/a
4	BACH1	chr2:189849679-189849710	K562	blood:	n/a	n/a
5	BATF	chr2:189843499-189843807	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:189843520-189843778	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:189843396-189843873	GM12878	blood:	n/a	n/a
8	BCL3	chr2:189843444-189843804	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:189843031-189843813	GM12878	blood:	n/a	n/a
10	CCNT2	chr2:189814185-189814456	K562	blood:	n/a	n/a
11	CEBPB	chr2:189837555-189837665	K562	blood:	n/a	n/a
12	CEBPB	chr2:189822384-189822731	IMR90	lung:	n/a	chr2:189822561-189822572
13	CEBPB	chr2:189817691-189817963	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:189802116-189802333	HepG2	liver:	n/a	chr2:189802178-189802189
15	CEBPB	chr2:189810513-189810759	HepG2	liver:	n/a	chr2:189810636-189810647
16	CEBPB	chr2:189849485-189849678	A549	lung:	n/a	n/a
17	CEBPB	chr2:189801990-189802401	IMR90	lung:	n/a	chr2:189802178-189802189
18	CEBPB	chr2:189848532-189849169	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:189834071-189834731	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:189822399-189822740	HepG2	liver:	n/a	chr2:189822561-189822572
21	CEBPB	chr2:189810524-189810725	IMR90	lung:	n/a	chr2:189810636-189810647
22	CEBPB	chr2:189827410-189827675	HepG2	liver:	n/a	chr2:189827520-189827531
23	CEBPB	chr2:189810547-189810723	A549	lung:	n/a	chr2:189810636-189810647
24	CEBPB	chr2:189837469-189837706	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:189834976-189835579	IMR90	lung:	n/a	chr2:189835050-189835063
26	CEBPB	chr2:189822393-189822712	A549	lung:	n/a	chr2:189822561-189822572
27	CTCF	chr2:189841460-189841610	HUVEC	blood vessel:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597
28	CTCF	chr2:189848300-189848450	HRPEpiC	eye:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
29	CTCF	chr2:189843100-189843250	AG10803	skin:	n/a	n/a
30	CTCF	chr2:189848267-189848410	GM13977	blood:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
31	CTCF	chr2:189843120-189843270	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr2:189841540-189841690	HRE	kidney:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597
33	CTCF	chr2:189841520-189841670	BJ	skin:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597
34	CTCF	chr2:189802120-189802270	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr2:189848280-189848430	HFF-Myc	foreskin:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
36	CTCF	chr2:189848999-189849214	Hela-S3	cervix:	n/a	chr2:189849095-189849116
37	CTCF	chr2:189848280-189848430	Caco-2	colon:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
38	CTCF	chr2:189841500-189841650	AG09319	gingival:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597
39	CTCF	chr2:189841620-189841770	HAc	cerebellar:	n/a	n/a
40	CTCF	chr2:189848236-189848433	HepG2	liver:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
41	CTCF	chr2:189801940-189802090	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr2:189840880-189841030	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:189848260-189848410	GM12865	blood:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
44	CTCF	chr2:189848960-189849110	AG04450	lung:	n/a	n/a
45	CTCF	chr2:189843060-189843210	NHLF	lung:	n/a	n/a
46	CTCF	chr2:189848230-189848437	Medullo	brain:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
47	CTCF	chr2:189841520-189841670	AG10803	skin:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597
48	CTCF	chr2:189843100-189843250	GM06990	blood:	n/a	n/a
49	CTCF	chr2:189849040-189849190	AG09309	skin:	n/a	chr2:189849095-189849116
50	CTCF	chr2:189848200-189848350	HA-sp	spinal cord:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:189839474-189839524	NHDF-neo	bronchial:	n/a
2	chr2:189839474-189839524	NHDF-neo	bronchial:	n/a
3	chr2:189837928-189837978	PFSK-1	brain:	n/a
4	chr2:189837928-189837978	K562	blood:	n/a
5	chr2:189839120-189839170	ovcar-3	ovarian:	n/a
6	chr2:189850571-189850621	NHBE	bronchial:	n/a
7	chr2:189839015-189839065	BJ	skin:	n/a
8	chr2:189850571-189850621	HCPEpiC	choroid plexus:	n/a
9	chr2:189839120-189839170	GM12891	blood:	n/a
10	chr2:189834269-189834319	U87	brain:	n/a
11	chr2:189839474-189839524	AG04450	lung:	fetal
12	chr2:189839474-189839524	HCF	heart:	n/a
13	chr2:189839015-189839065	AG04450	lung:	fetal
14	chr2:189839015-189839065	PFSK-1	brain:	n/a
15	chr2:189839474-189839524	Hepatocyte	liver:	n/a
16	chr2:189839015-189839065	IMR90	lung:	fetal
17	chr2:189839015-189839065	Hela-S3	cervix:	n/a
18	chr2:189837928-189837978	GM19239	blood:	n/a
19	chr2:189839015-189839065	H1-hESC	embryonic stem cell:	embryo
20	chr2:189839120-189839170	NHDF-neo	bronchial:	n/a
21	chr2:189834269-189834319	BE2_C	brain:	n/a
22	chr2:189839015-189839065	AoSMC	blood vessel:	n/a
23	chr2:189839120-189839170	T-47D	breast:	n/a
24	chr2:189850571-189850621	NH-A	brain:	n/a
25	chr2:189837928-189837978	HRCEpiC	kidney:	n/a
26	chr2:189839474-189839524	U87	brain:	n/a
27	chr2:189839015-189839065	HRCEpiC	kidney:	n/a
28	chr2:189839015-189839065	HEK293	kidney:	embryo
29	chr2:189837928-189837978	RPTEC	kidney:	n/a
30	chr2:189839015-189839065	GM06990	blood:	n/a
31	chr2:189839015-189839065	LNCaP	prostate:	n/a
32	chr2:189834269-189834319	HEK293	kidney:	embryo
33	chr2:189837928-189837978	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:189837928-189837978	IMR90	lung:	fetal
35	chr2:189834269-189834319	NT2-D1	testis:	n/a
36	chr2:189837928-189837978	Jurkat	blood:	n/a
37	chr2:189837928-189837978	AG10803	skin:	n/a
38	chr2:189850571-189850621	GM12891	blood:	n/a
39	chr2:189837928-189837978	LNCaP	prostate:	n/a
40	chr2:189839015-189839065	A549	lung:	n/a
41	chr2:189839015-189839065	HCT-116	colon:	n/a
42	chr2:189834269-189834319	AoSMC	blood vessel:	n/a
43	chr2:189837928-189837978	T-47D	breast:	n/a
44	chr2:189839015-189839065	HUVEC	blood vessel:	n/a
45	chr2:189839120-189839170	HNPCEpiC	eye:	n/a
46	chr2:189839015-189839065	HRE	kidney:	n/a
47	chr2:189834269-189834319	ovcar-3	ovarian:	n/a
48	chr2:189839474-189839524	GM12891	blood:	n/a
49	chr2:189837928-189837978	H1-hESC	embryonic stem cell:	embryo
50	chr2:189839474-189839524	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:189848219..189848800-chr2:190276497..190277312,2	MCF-7	breast:
2	chr2:189388967..189389813-chr2:189842832..189843620,3	MCF-7	breast:
3	chr2:189389424..189389930-chr2:189841189..189841702,2	MCF-7	breast:
4	chr2:188459276..188460160-chr2:189841055..189841647,2	MCF-7	breast:
5	chr2:189465598..189467415-chr2:189847399..189849894,2	MCF-7	breast:
6	chr2:189822907..189823896-chr8:96619389..96620128,2	MCF-7	breast:
7	chr2:189843846..189845833-chr2:189848371..189850816,2	K562	blood:
8	chr2:189849262..189851265-chr2:189851542..189854419,2	MCF-7	breast:
9	chr2:189843846..189845833-chr2:189848371..189850816,2	K562	blood:
10	chr2:189840465..189844920-chr2:189846827..189849857,3	MCF-7	breast:
11	chr2:189378368..189379278-chr2:189848607..189850003,3	MCF-7	breast:
12	chr2:189652355..189655667-chr2:189836980..189839231,3	MCF-7	breast:
13	chr2:189467608..189469705-chr2:189839952..189841474,2	MCF-7	breast:
14	chr2:189849262..189851265-chr2:189851542..189854419,2	MCF-7	breast:
15	chr2:189460620..189463074-chr2:189843714..189846986,3	MCF-7	breast:
16	chr2:189468604..189471181-chr2:189847592..189850287,2	MCF-7	breast:
17	chr2:189847939..189848875-chr2:190211912..190212800,2	MCF-7	breast:
18	chr2:189630030..189631002-chr2:189840905..189842141,9	MCF-7	breast:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1245a	chr2:189842862-189842882	MIMAT0005897
hsa-miR-1245b-3p	chr2:189842825-189842846	MIMAT0019951
hsa-miR-1245b-5p	chr2:189842859-189842879	MIMAT0019950

Variant related genes	Relation type
MIR1245A	TF binding region
COL3A1	TF binding region
MIR1245A	CpG island
COL3A1	CpG island
ENSG00000174325	chromatin interactions
ENSG00000221502	chromatin interactions
BRCA2	Mature miRNA region

Extended variants
information (count: 2027 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:2027 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16830844	chr2:189799499-189799500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs180943317	chr2:189799531-189799532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183525205	chr2:189799532-189799533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147725698	chr2:189799550-189799551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553012040	chr2:189799551-189799552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373239448	chr2:189799555-189799556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376964521	chr2:189799569-189799570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs377139052	chr2:189799582-189799583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140886154	chr2:189799603-189799604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544443881	chr2:189799659-189799660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs4667253	chr2:189799682-189799683	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs575729963	chr2:189799728-189799729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546000674	chr2:189799736-189799737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs75461128	chr2:189799853-189799854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528501660	chr2:189799887-189799888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149821194	chr2:189799978-189799979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533471876	chr2:189800053-189800054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190674459	chr2:189800125-189800126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575430509	chr2:189800160-189800161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529443340	chr2:189800198-189800199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10497694	chr2:189800211-189800212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181928604	chr2:189800281-189800282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539492093	chr2:189800327-189800328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs67494960	chr2:189800375-189800376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs397692549	chr2:189800378-189800379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201464782	chr2:189800379-189800380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17241561	chr2:189800385-189800386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
28	rs111540830	chr2:189800388-189800389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144962561	chr2:189800470-189800471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561019826	chr2:189800501-189800502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560777695	chr2:189800511-189800512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533584067	chr2:189800512-189800513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112664310	chr2:189800519-189800520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555241187	chr2:189800553-189800554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567580945	chr2:189800569-189800570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537630335	chr2:189800603-189800604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556292322	chr2:189800644-189800645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs13009963	chr2:189800662-189800663	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs112058889	chr2:189800685-189800686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs367576333	chr2:189800715-189800716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573269317	chr2:189800724-189800725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540657340	chr2:189800740-189800741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs62181699	chr2:189800741-189800742	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs187378139	chr2:189800752-189800753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549832688	chr2:189800761-189800762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs13010226	chr2:189800774-189800775	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs58004989	chr2:189800790-189800791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11284244	chr2:189800794-189800795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76815565	chr2:189800795-189800796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs398080908	chr2:189800804-189800805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	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
Breast cancer	21364760	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Colorectal cancer	16912164	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:189794400-189802000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr2:189796400-189801600	Weak transcription	Osteobl	bone
3	chr2:189796600-189801400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:189796600-189801600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:189796600-189802000	Weak transcription	NHDF-Ad	bronchial
6	chr2:189799400-189802400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:189801400-189802400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:189801600-189802200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr2:189801600-189802400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:189801600-189802400	Enhancers	Osteobl	bone
11	chr2:189802000-189802200	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr2:189802000-189802400	Enhancers	Adipose Nuclei	Adipose
13	chr2:189802000-189802800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr2:189802000-189803000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr2:189802000-189803200	Enhancers	Colon Smooth Muscle	Colon
16	chr2:189802000-189803200	Enhancers	NHDF-Ad	bronchial
17	chr2:189802200-189802800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:189802200-189803200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:189802200-189805000	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr2:189802400-189803200	Flanking Active TSS	Adipose Nuclei	Adipose
21	chr2:189802400-189803200	Enhancers	Aorta	Aorta
22	chr2:189802400-189803200	Flanking Active TSS	Osteobl	bone
23	chr2:189802400-189803400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:189802400-189803400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr2:189802400-189803800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:189802600-189803200	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr2:189802800-189803200	Enhancers	Right Atrium	heart
28	chr2:189802800-189805000	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr2:189803000-189805000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr2:189803200-189804800	Weak transcription	Adipose Nuclei	Adipose
31	chr2:189803200-189804800	Weak transcription	NHDF-Ad	bronchial
32	chr2:189803200-189805200	Enhancers	Osteobl	bone
33	chr2:189803200-189805600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr2:189803200-189807200	Weak transcription	Aorta	Aorta
35	chr2:189803400-189804200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:189803400-189804800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr2:189803800-189804400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr2:189804200-189804600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr2:189804400-189805200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr2:189804600-189804800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr2:189804800-189805200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr2:189804800-189805200	Enhancers	Adipose Nuclei	Adipose
43	chr2:189804800-189805200	Active TSS	Fetal Lung	lung
44	chr2:189804800-189805200	Flanking Active TSS	NHDF-Ad	bronchial
45	chr2:189804800-189805400	Enhancers	HUVEC	blood vessel
46	chr2:189804800-189805600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr2:189805000-189805200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:189805000-189805200	Enhancers	Muscle Satellite Cultured Cells	--
49	chr2:189805000-189805200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr2:189805000-189805200	Enhancers	Right Ventricle	heart

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