Variant report

Variant	nsv834025
Chromosome Location	chr2:52514959-52693049
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	ATF2	chr2:52667276-52667711	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr2:52667277-52667714	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:52565069-52565261	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:52562997-52563330	H1-hESC	embryonic stem cell:	n/a	chr2:52563100-52563114
5	BCL11A	chr2:52667354-52667508	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr2:52667333-52667627	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr2:52675363-52675413	K562	blood:	n/a	n/a
8	BHLHE40	chr2:52675296-52675528	GM12878	blood:	n/a	n/a
9	BRCA1	chr2:52656816-52657285	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr2:52554738-52555164	HCT-116	colon:	n/a	n/a
11	CEBPB	chr2:52562807-52563121	A549	lung:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
12	CEBPB	chr2:52667357-52667802	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:52669525-52669824	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:52679211-52679275	A549	lung:	n/a	n/a
15	CEBPB	chr2:52516890-52517212	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:52682200-52682504	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:52570882-52571236	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr2:52666378-52666692	H1-hESC	embryonic stem cell:	n/a	chr2:52666669-52666680 chr2:52666671-52666680 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666671-52666682
19	CEBPB	chr2:52682169-52682476	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:52656730-52657359	IMR90	lung:	n/a	chr2:52657151-52657160 chr2:52657086-52657099 chr2:52657149-52657162 chr2:52657151-52657162 chr2:52657151-52657160 chr2:52657149-52657162 chr2:52657151-52657160 chr2:52657151-52657160 chr2:52657149-52657160
21	CEBPB	chr2:52616319-52616570	HepG2	liver:	n/a	chr2:52616446-52616457 chr2:52616447-52616458 chr2:52616446-52616459
22	CEBPB	chr2:52562730-52563288	ECC-1	luminal epithelium:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52563266-52563277 chr2:52562956-52562967
23	CEBPB	chr2:52682177-52682409	A549	lung:	n/a	n/a
24	CEBPB	chr2:52570199-52570514	A549	lung:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
25	CEBPB	chr2:52570208-52570547	Hela-S3	cervix:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
26	CEBPB	chr2:52623783-52624296	HepG2	liver:	n/a	chr2:52624106-52624117
27	CEBPB	chr2:52683698-52683958	A549	lung:	n/a	n/a
28	CEBPB	chr2:52568912-52569271	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:52570177-52570534	HepG2	liver:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
30	CEBPB	chr2:52683689-52684029	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:52562815-52563192	IMR90	lung:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
32	CEBPB	chr2:52666507-52666820	HepG2	liver:	n/a	chr2:52666669-52666680 chr2:52666671-52666680 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666671-52666682
33	CEBPB	chr2:52667215-52667804	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:52656984-52657337	A549	lung:	n/a	chr2:52657151-52657160 chr2:52657086-52657099 chr2:52657149-52657162 chr2:52657151-52657162 chr2:52657151-52657160 chr2:52657149-52657162 chr2:52657151-52657160 chr2:52657151-52657160 chr2:52657149-52657160
35	CEBPB	chr2:52569009-52569163	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:52669548-52669831	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:52562773-52563118	HepG2	liver:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
38	CEBPB	chr2:52516875-52517234	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:52657012-52657230	H1-hESC	embryonic stem cell:	n/a	chr2:52657151-52657160 chr2:52657086-52657099 chr2:52657149-52657162 chr2:52657151-52657162 chr2:52657151-52657160 chr2:52657149-52657162 chr2:52657151-52657160 chr2:52657151-52657160 chr2:52657149-52657160
40	CEBPB	chr2:52516417-52516634	HepG2	liver:	n/a	chr2:52516470-52516481
41	CEBPB	chr2:52568887-52569285	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:52692381-52692934	Hela-S3	cervix:	n/a	chr2:52692711-52692723 chr2:52692721-52692732
43	CEBPB	chr2:52562704-52563282	ECC-1	luminal epithelium:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52563266-52563277 chr2:52562956-52562967
44	CEBPB	chr2:52562875-52563266	H1-hESC	embryonic stem cell:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
45	CEBPB	chr2:52650239-52651116	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr2:52569536-52570532	IMR90	lung:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
47	CEBPB	chr2:52669548-52669834	A549	lung:	n/a	n/a
48	CEBPB	chr2:52570175-52570518	H1-hESC	embryonic stem cell:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
49	CEBPB	chr2:52656987-52657341	HepG2	liver:	n/a	chr2:52657151-52657160 chr2:52657086-52657099 chr2:52657149-52657162 chr2:52657151-52657162 chr2:52657151-52657160 chr2:52657149-52657162 chr2:52657151-52657160 chr2:52657151-52657160 chr2:52657149-52657160
50	CEBPB	chr2:52666489-52666836	Hela-S3	cervix:	n/a	chr2:52666669-52666680 chr2:52666671-52666680 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666671-52666682

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52656979-52657029	AG04449	skin:	fetal
2	chr2:52656979-52657029	AG04449	skin:	fetal
3	chr2:52571550-52571600	NT2-D1	testis:	n/a
4	chr2:52571550-52571600	NHBE	bronchial:	n/a
5	chr2:52571550-52571600	RPTEC	kidney:	n/a
6	chr2:52614831-52614881	HL-60	blood:	n/a
7	chr2:52571550-52571600	CMK	blood:	n/a
8	chr2:52656979-52657029	HRCEpiC	kidney:	n/a
9	chr2:52656979-52657029	HRPEpiC	eye:	n/a
10	chr2:52571550-52571600	Hepatocyte	liver:	n/a
11	chr2:52571550-52571600	U87	brain:	n/a
12	chr2:52614831-52614881	HIPEpiC	eye:	n/a
13	chr2:52614831-52614881	GM06990	blood:	n/a
14	chr2:52656979-52657029	IMR90	lung:	fetal
15	chr2:52571550-52571600	HCPEpiC	choroid plexus:	n/a
16	chr2:52656979-52657029	HCPEpiC	choroid plexus:	n/a
17	chr2:52571550-52571600	AG10803	skin:	n/a
18	chr2:52571550-52571600	HEK293	kidney:	embryo
19	chr2:52656979-52657029	BJ	skin:	n/a
20	chr2:52614831-52614881	ECC-1	luminal epithelium:	n/a
21	chr2:52614831-52614881	HCT-116	colon:	n/a
22	chr2:52656979-52657029	RPTEC	kidney:	n/a
23	chr2:52571550-52571600	HNPCEpiC	eye:	n/a
24	chr2:52656979-52657029	HMEC	breast:	n/a
25	chr2:52571550-52571600	K562	blood:	n/a
26	chr2:52656979-52657029	AoSMC	blood vessel:	n/a
27	chr2:52571550-52571600	HRE	kidney:	n/a
28	chr2:52571550-52571600	GM19239	blood:	n/a
29	chr2:52614831-52614881	GM19239	blood:	n/a
30	chr2:52614831-52614881	NHDF-neo	bronchial:	n/a
31	chr2:52656979-52657029	Jurkat	blood:	n/a
32	chr2:52571550-52571600	BJ	skin:	n/a
33	chr2:52656979-52657029	LNCaP	prostate:	n/a
34	chr2:52614831-52614881	SK-N-MC	brain:	n/a
35	chr2:52656979-52657029	SKMC	muscle:	n/a
36	chr2:52571550-52571600	HepG2	liver:	n/a
37	chr2:52656979-52657029	HEEpiC	esophagus:	n/a
38	chr2:52614831-52614881	SK-N-SH	brain:	n/a
39	chr2:52571550-52571600	HL-60	blood:	n/a
40	chr2:52656979-52657029	T-47D	breast:	n/a
41	chr2:52656979-52657029	AG04450	lung:	fetal
42	chr2:52656979-52657029	NHBE	bronchial:	n/a
43	chr2:52571550-52571600	NHDF-neo	bronchial:	n/a
44	chr2:52571550-52571600	LNCaP	prostate:	n/a
45	chr2:52614831-52614881	IMR90	lung:	fetal
46	chr2:52571550-52571600	PFSK-1	brain:	n/a
47	chr2:52656979-52657029	AG09309	skin:	n/a
48	chr2:52614831-52614881	ovcar-3	ovarian:	n/a
49	chr2:52571550-52571600	HRCEpiC	kidney:	n/a
50	chr2:52614831-52614881	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:56708428..56710649-chr2:52687376..52688939,2	MCF-7	breast:
2	chr2:52521422..52524399-chr2:52528510..52532522,3	K562	blood:
3	chr2:52644535..52645157-chr2:52839947..52840842,2	MCF-7	breast:
4	chr2:52521422..52524399-chr2:52528510..52532522,3	K562	blood:
5	chr2:52618576..52620644-chr2:52620820..52623618,2	MCF-7	breast:
6	chr2:52618576..52620644-chr2:52620820..52623618,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-4	chr2:52580012-52580100	ENSG00000231918.1
2	lnc-CHAC2-4	chr2:52543370-52543438	ENSG00000231918.1
3	lnc-CHAC2-3	chr2:52616601-52617150	XLOC_001468
4	lnc-ASB3-11	chr2:52581186-52581394	NONHSAT070669
5	lnc-CHAC2-4	chr2:52576463-52578424	ENSG00000231918.1
6	lnc-CHAC2-4	chr2:52634116-52635055	ENSG00000231918.1
7	lnc-ASB3-11	chr2:52576407-52576478	NONHSAT070669
8	lnc-ASB3-11	chr2:52579245-52579427	NONHSAT070669
9	lnc-ASB3-11	chr2:52575330-52575504	NONHSAT070669
10	lnc-CHAC2-3	chr2:52600256-52600309	XLOC_001468

Variant related genes	Relation type
ENSG00000225444	TF binding region
ENSG00000202195	TF binding region
ENSG00000225444	CpG island
ENSG00000202195	CpG island
ENSG00000212195	chromatin interactions

Extended variants
information (count: 6265 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:6265 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180719668	chr2:52515008-52515009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541686109	chr2:52515010-52515011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565748838	chr2:52515012-52515013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554943646	chr2:52515033-52515034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545097483	chr2:52515036-52515037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200106449	chr2:52515087-52515088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558630962	chr2:52515171-52515172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143132080	chr2:52515180-52515181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs74547585	chr2:52515201-52515202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369760200	chr2:52515214-52515215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184437759	chr2:52515246-52515247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372816074	chr2:52515253-52515254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543647029	chr2:52515274-52515275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562464012	chr2:52515275-52515276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563955026	chr2:52515278-52515279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531335067	chr2:52515281-52515282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531259504	chr2:52515290-52515291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72885581	chr2:52515364-52515365	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs565007711	chr2:52515385-52515386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372933260	chr2:52515499-52515500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377237402	chr2:52515582-52515583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547548622	chr2:52515591-52515592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370067016	chr2:52515612-52515613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7561300	chr2:52515637-52515638	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs564505138	chr2:52515644-52515645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537073138	chr2:52515646-52515647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188342583	chr2:52515660-52515661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549714356	chr2:52515705-52515706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115778599	chr2:52515719-52515720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7588155	chr2:52515792-52515793	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs558751983	chr2:52515808-52515809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371332291	chr2:52515860-52515861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181826914	chr2:52515861-52515862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186322924	chr2:52515906-52515907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72885587	chr2:52515933-52515934	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs575131615	chr2:52515941-52515942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72885588	chr2:52515948-52515949	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs563980479	chr2:52516003-52516004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576072643	chr2:52516043-52516044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138647580	chr2:52516095-52516096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10181395	chr2:52516105-52516106	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs527366577	chr2:52516120-52516121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547217517	chr2:52516207-52516208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561135685	chr2:52516216-52516217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114417126	chr2:52516237-52516238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569866569	chr2:52516247-52516248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs72885589	chr2:52516258-52516259	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs569633693	chr2:52516272-52516273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10205415	chr2:52516309-52516310	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs552526437	chr2:52516320-52516321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
small cell lung cancer	20016488	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:440 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52513400-52515400	Enhancers	Fetal Intestine Small	intestine
2	chr2:52513400-52516400	Enhancers	Fetal Intestine Large	intestine
3	chr2:52513600-52516000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:52514200-52516400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr2:52514400-52515200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:52514600-52515200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr2:52514600-52515400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr2:52514800-52515400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr2:52515200-52515400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:52515200-52523000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr2:52515400-52516400	Weak transcription	Fetal Intestine Small	intestine
12	chr2:52515800-52516400	Enhancers	Fetal Heart	heart
13	chr2:52516000-52519800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr2:52516400-52516600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr2:52516400-52516600	Enhancers	Fetal Intestine Small	intestine
16	chr2:52519000-52519200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:52519000-52520800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr2:52519200-52520200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr2:52519200-52520200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:52519200-52521600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr2:52519600-52520600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr2:52519600-52520800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr2:52519800-52521000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:52520000-52520200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:52520000-52521200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:52520200-52521400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:52520600-52521600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr2:52520800-52521200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr2:52520800-52522400	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr2:52521000-52522400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:52521200-52523800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:52521400-52522000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr2:52521400-52522200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr2:52521600-52522200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr2:52521600-52524800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr2:52522200-52522800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr2:52522400-52523000	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr2:52522800-52523000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:52522800-52523200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr2:52523000-52523800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr2:52524800-52526000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
42	chr2:52535800-52536400	Enhancers	Fetal Intestine Large	intestine
43	chr2:52537200-52537800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr2:52537600-52538800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:52537600-52539600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr2:52537800-52538800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr2:52537800-52540000	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr2:52538000-52539000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr2:52538200-52539600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr2:52538400-52538600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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