Variant report

Variant	nsv1007170
Chromosome Location	chr2:52681191-52703416
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	CEBPB	chr2:52698901-52699369	A549	lung:	n/a	chr2:52699035-52699046
2	CEBPB	chr2:52702578-52703057	IMR90	lung:	n/a	chr2:52702675-52702692 chr2:52702847-52702858 chr2:52702676-52702689 chr2:52702676-52702687 chr2:52702646-52702657 chr2:52702907-52702918 chr2:52703014-52703026
3	CEBPB	chr2:52692381-52692934	Hela-S3	cervix:	n/a	chr2:52692711-52692723 chr2:52692721-52692732
4	CEBPB	chr2:52683698-52683958	A549	lung:	n/a	n/a
5	CEBPB	chr2:52698898-52699465	HepG2	liver:	n/a	chr2:52699035-52699046
6	CEBPB	chr2:52682200-52682504	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:52702812-52703040	A549	lung:	n/a	chr2:52702847-52702858 chr2:52702907-52702918 chr2:52703014-52703026
8	CEBPB	chr2:52682177-52682409	A549	lung:	n/a	n/a
9	CEBPB	chr2:52682180-52682454	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr2:52702580-52703046	HepG2	liver:	n/a	chr2:52702675-52702692 chr2:52702847-52702858 chr2:52702676-52702689 chr2:52702676-52702687 chr2:52702646-52702657 chr2:52702907-52702918 chr2:52703014-52703026
11	CEBPB	chr2:52699331-52699366	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:52683689-52684029	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:52682169-52682476	IMR90	lung:	n/a	n/a
14	CHD2	chr2:52697733-52697749	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr2:52683920-52684070	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr2:52684785-52684804	LNCaP	prostate:	n/a	n/a
17	CTCF	chr2:52701720-52701870	Caco-2	colon:	n/a	n/a
18	CTCF	chr2:52701560-52701710	Caco-2	colon:	n/a	n/a
19	CTCF	chr2:52684764-52684817	GM10266	blood:	n/a	n/a
20	CTCF	chr2:52684738-52684835	GM10248	blood:	n/a	n/a
21	CTCF	chr2:52684000-52684150	HCPEpiC	choroid plexus:	n/a	n/a
22	EP300	chr2:52693206-52693207	GM12878	blood:	n/a	n/a
23	EP300	chr2:52692584-52692937	Hela-S3	cervix:	n/a	chr2:52692839-52692848 chr2:52692838-52692847
24	FOS	chr2:52702589-52702949	MCF10A-Er-Src	breast:	n/a	chr2:52702666-52702674
25	FOS	chr2:52702484-52703010	MCF10A-Er-Src	breast:	n/a	chr2:52702666-52702674
26	FOS	chr2:52702533-52702974	MCF10A-Er-Src	breast:	n/a	chr2:52702666-52702674
27	FOS	chr2:52702493-52703031	MCF10A-Er-Src	breast:	n/a	chr2:52702666-52702674
28	JUN	chr2:52684042-52684375	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAFF	chr2:52698966-52699166	HepG2	liver:	n/a	n/a
30	MAFK	chr2:52702917-52702961	HepG2	liver:	n/a	chr2:52702922-52702933 chr2:52702921-52702937 chr2:52702922-52702933 chr2:52702920-52702934 chr2:52702921-52702932 chr2:52702921-52702936 chr2:52702921-52702932
31	MAFK	chr2:52702870-52703007	HepG2	liver:	n/a	chr2:52702922-52702933 chr2:52702921-52702937 chr2:52702922-52702933 chr2:52702920-52702934 chr2:52702921-52702932 chr2:52702921-52702936 chr2:52702921-52702932
32	MAFK	chr2:52694501-52694725	HepG2	liver:	n/a	chr2:52694587-52694602
33	MAFK	chr2:52699029-52699178	HepG2	liver:	n/a	n/a
34	MAFK	chr2:52685258-52685347	H1-hESC	embryonic stem cell:	n/a	n/a
35	MAFK	chr2:52694537-52694664	HepG2	liver:	n/a	chr2:52694587-52694602
36	MAFK	chr2:52682132-52682397	HepG2	liver:	n/a	chr2:52682258-52682274 chr2:52682263-52682274 chr2:52682263-52682274
37	MAFK	chr2:52698944-52699197	HepG2	liver:	n/a	n/a
38	MYC	chr2:52684700-52684823	HUVEC	blood vessel:	n/a	n/a
39	NRF1	chr2:52690775-52690949	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr2:52683543-52683600	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr2:52694392-52694612	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr2:52689293-52689297	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr2:52681459-52681563	A549	lung:	n/a	n/a
44	POLR2A	chr2:52683022-52683068	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr2:52694400-52694675	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr2:52702870-52703034	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr2:52701563-52701583	A549	lung:	n/a	n/a
48	POLR2A	chr2:52685457-52685477	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr2:52681440-52681457	A549	lung:	n/a	n/a
50	POLR2A	chr2:52697323-52697398	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52695221-52695271	Hepatocyte	liver:	n/a
2	chr2:52695221-52695271	NB4	blood:	n/a
3	chr2:52695221-52695271	ovcar-3	ovarian:	n/a
4	chr2:52695221-52695271	A549	lung:	n/a
5	chr2:52695221-52695271	AG09309	skin:	n/a
6	chr2:52695221-52695271	CMK	blood:	n/a
7	chr2:52695221-52695271	HMEC	breast:	n/a
8	chr2:52695221-52695271	NT2-D1	testis:	n/a
9	chr2:52695221-52695271	PANC-1	pancreas:	n/a
10	chr2:52695221-52695271	SK-N-SH_RA	brain:	n/a
11	chr2:52695221-52695271	AG10803	skin:	n/a
12	chr2:52695221-52695271	HEK293	kidney:	embryo
13	chr2:52695221-52695271	AoSMC	blood vessel:	n/a
14	chr2:52695221-52695271	HCPEpiC	choroid plexus:	n/a
15	chr2:52695221-52695271	NH-A	brain:	n/a
16	chr2:52695221-52695271	RPTEC	kidney:	n/a
17	chr2:52695221-52695271	SAEC	small airway:	n/a
18	chr2:52695221-52695271	Hela-S3	cervix:	n/a
19	chr2:52695221-52695271	LNCaP	prostate:	n/a
20	chr2:52695221-52695271	SKMC	muscle:	n/a
21	chr2:52695221-52695271	GM12891	blood:	n/a
22	chr2:52695221-52695271	AG04449	skin:	fetal
23	chr2:52695221-52695271	GM12878	blood:	n/a
24	chr2:52695221-52695271	HL-60	blood:	n/a
25	chr2:52695221-52695271	GM06990	blood:	n/a
26	chr2:52695221-52695271	GM19239	blood:	n/a
27	chr2:52695221-52695271	BE2_C	brain:	n/a
28	chr2:52695221-52695271	AG09319	gingival:	n/a
29	chr2:52695221-52695271	H1-hESC	embryonic stem cell:	embryo
30	chr2:52695221-52695271	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:52695221-52695271	HEEpiC	esophagus:	n/a
32	chr2:52695221-52695271	MCF10A-Er-Src	breast:	n/a
33	chr2:52695221-52695271	T-47D	breast:	n/a
34	chr2:52695221-52695271	BJ	skin:	n/a
35	chr2:52695221-52695271	HIPEpiC	eye:	n/a
36	chr2:52695221-52695271	ProgFib	skin:	n/a
37	chr2:52695221-52695271	Jurkat	blood:	n/a
38	chr2:52695221-52695271	MCF-7	breast:	n/a
39	chr2:52695221-52695271	PFSK-1	brain:	n/a
40	chr2:52695221-52695271	AG04450	lung:	fetal
41	chr2:52695221-52695271	ECC-1	luminal epithelium:	n/a
42	chr2:52695221-52695271	HepG2	liver:	n/a
43	chr2:52695221-52695271	HAEpiC	amniotic membrane:	n/a
44	chr2:52695221-52695271	NHDF-neo	bronchial:	n/a
45	chr2:52695221-52695271	HCT-116	colon:	n/a
46	chr2:52695221-52695271	HRPEpiC	eye:	n/a
47	chr2:52695221-52695271	NHBE	bronchial:	n/a
48	chr2:52695221-52695271	HUVEC	blood vessel:	n/a
49	chr2:52695221-52695271	Caco-2	colon:	n/a
50	chr2:52695221-52695271	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:56708428..56710649-chr2:52687376..52688939,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB3-10	chr2:52701211-52701549	NONHSAT070672

Variant related genes	Relation type
ENSG00000225842	TF binding region
ENSG00000225842	CpG island
ENSG00000212195	chromatin interactions

Extended variants
information (count: 1068 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1068 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577998139	chr2:52681210-52681211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs540488496	chr2:52681224-52681225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560468635	chr2:52681227-52681228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532580164	chr2:52681262-52681263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557978879	chr2:52681277-52681278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189308596	chr2:52681280-52681281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562524173	chr2:52681283-52681284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7582083	chr2:52681313-52681314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4588226	chr2:52681326-52681327	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs143300466	chr2:52681359-52681360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571459569	chr2:52681374-52681375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534132138	chr2:52681401-52681402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147151018	chr2:52681402-52681403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139461798	chr2:52681438-52681439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149233064	chr2:52681488-52681489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555375394	chr2:52681505-52681506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2032992	chr2:52681515-52681516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575242142	chr2:52681533-52681534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537993097	chr2:52681562-52681563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568679234	chr2:52681585-52681586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577873922	chr2:52681628-52681629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181933327	chr2:52681634-52681635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144501646	chr2:52681636-52681637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368240417	chr2:52681648-52681649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573909833	chr2:52681651-52681652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113326861	chr2:52681664-52681665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542644488	chr2:52681665-52681666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562944882	chr2:52681684-52681685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531610473	chr2:52681757-52681758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185990143	chr2:52681800-52681801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536305297	chr2:52681835-52681836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545057291	chr2:52681853-52681854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191653644	chr2:52681963-52681964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371243272	chr2:52681986-52681987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs527851459	chr2:52682009-52682010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533131782	chr2:52682020-52682021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148420760	chr2:52682090-52682091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554185689	chr2:52682099-52682100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530466109	chr2:52682139-52682140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548700863	chr2:52682187-52682188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183810201	chr2:52682188-52682189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556339194	chr2:52682202-52682203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186272523	chr2:52682294-52682295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191626957	chr2:52682314-52682315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575937674	chr2:52682338-52682339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545017822	chr2:52682360-52682361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182182498	chr2:52682364-52682365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554046839	chr2:52682367-52682368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573847895	chr2:52682412-52682413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186679729	chr2:52682424-52682425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52674200-52682800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr2:52680400-52684400	Enhancers	Liver	Liver
3	chr2:52681800-52684600	Enhancers	Fetal Intestine Large	intestine
4	chr2:52682400-52684600	Enhancers	Fetal Intestine Small	intestine
5	chr2:52682800-52683000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr2:52683000-52683800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr2:52683200-52684200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr2:52683400-52684200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:52683400-52684200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr2:52683400-52684400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr2:52683400-52684400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr2:52683400-52685400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr2:52683600-52684000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:52683600-52684000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr2:52683600-52684400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr2:52683600-52684400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr2:52683600-52685400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr2:52683600-52686200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr2:52683800-52684200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr2:52683800-52684200	Enhancers	H9 Cell Line	embryonic stem cell
21	chr2:52684000-52685200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr2:52684000-52694000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:52684200-52685200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr2:52684200-52685200	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr2:52684200-52685200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr2:52684200-52692200	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr2:52684400-52685200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr2:52684400-52689200	Weak transcription	Liver	Liver
29	chr2:52684400-52690800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr2:52684400-52694400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr2:52685200-52685400	Enhancers	H9 Cell Line	embryonic stem cell
32	chr2:52685200-52686000	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr2:52685200-52686200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr2:52685200-52686200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr2:52685400-52694000	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr2:52687200-52688000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:52689200-52690600	Enhancers	Liver	Liver
38	chr2:52690600-52691000	Flanking Active TSS	Liver	Liver
39	chr2:52690800-52691000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr2:52691000-52691200	Enhancers	Liver	Liver
41	chr2:52691000-52698000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr2:52692000-52692200	Enhancers	Hela-S3	cervix
43	chr2:52692000-52692800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:52692000-52693000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr2:52692200-52692400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr2:52692200-52692600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:52692200-52692800	Flanking Active TSS	Hela-S3	cervix
48	chr2:52692200-52693000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr2:52692400-52694200	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr2:52692600-52693000	Enhancers	NH-A	brain

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