Variant report

Variant	nsv536071
Chromosome Location	chr2:183666013-183777604
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:776)
CpG islands
(count:1160)
Chromatin interactive
region (count:53)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:776 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:183668859-183669300	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:183679569-183679767	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:183755294-183756486	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:183731010-183731021	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:183772253-183772399	K562	blood:	n/a	n/a
6	ARID3A	chr2:183764997-183765224	HepG2	liver:	n/a	n/a
7	ATF1	chr2:183725934-183726010	K562	blood:	n/a	n/a
8	BACH1	chr2:183732098-183732408	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:183771914-183772348	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:183730971-183731063	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr2:183769640-183769883	GM12878	blood:	n/a	chr2:183769744-183769755 chr2:183769745-183769755
12	BCL11A	chr2:183683644-183683969	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr2:183735041-183735273	K562	blood:	n/a	n/a
14	BHLHE40	chr2:183763855-183763984	K562	blood:	n/a	n/a
15	BRCA1	chr2:183731451-183731729	HepG2	liver:	n/a	n/a
16	BRCA1	chr2:183732940-183733129	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr2:183679511-183679776	HepG2	liver:	n/a	n/a
18	CBX3	chr2:183771989-183772370	K562	blood:	n/a	n/a
19	CCNT2	chr2:183735166-183735220	K562	blood:	n/a	n/a
20	CEBPB	chr2:183731254-183731648	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr2:183731437-183731586	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:183777052-183777263	ECC-1	luminal epithelium:	n/a	chr2:183777080-183777093
23	CEBPB	chr2:183756376-183756724	K562	blood:	n/a	chr2:183756554-183756567 chr2:183756555-183756566 chr2:183756554-183756567
24	CEBPB	chr2:183726801-183727122	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:183751918-183752113	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:183756472-183756651	H1-hESC	embryonic stem cell:	n/a	chr2:183756554-183756567 chr2:183756555-183756566 chr2:183756554-183756567
27	CEBPB	chr2:183684963-183685265	IMR90	lung:	n/a	chr2:183685096-183685107
28	CEBPB	chr2:183770567-183770691	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr2:183756389-183756697	A549	lung:	n/a	chr2:183756554-183756567 chr2:183756555-183756566 chr2:183756554-183756567
30	CEBPB	chr2:183765023-183765164	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:183726813-183727013	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:183748257-183748584	IMR90	lung:	n/a	chr2:183748400-183748411
33	CEBPB	chr2:183676867-183676952	HepG2	liver:	n/a	chr2:183676879-183676890
34	CEBPB	chr2:183679609-183679973	HepG2	liver:	n/a	chr2:183679810-183679823 chr2:183679811-183679822
35	CEBPB	chr2:183685030-183685198	A549	lung:	n/a	chr2:183685096-183685107
36	CEBPB	chr2:183734241-183734433	HepG2	liver:	n/a	chr2:183734351-183734362
37	CEBPB	chr2:183684952-183685196	HepG2	liver:	n/a	chr2:183685096-183685107
38	CEBPB	chr2:183755695-183756066	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:183676807-183676931	H1-hESC	embryonic stem cell:	n/a	chr2:183676879-183676890
40	CEBPB	chr2:183756388-183756711	HepG2	liver:	n/a	chr2:183756554-183756567 chr2:183756555-183756566 chr2:183756554-183756567
41	CEBPB	chr2:183676829-183676918	K562	blood:	n/a	chr2:183676879-183676890
42	CEBPB	chr2:183755656-183756008	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:183731324-183731676	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:183732886-183733095	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:183741611-183741653	HepG2	liver:	n/a	chr2:183741618-183741629
46	CEBPB	chr2:183756383-183756726	IMR90	lung:	n/a	chr2:183756554-183756567 chr2:183756555-183756566 chr2:183756554-183756567
47	CEBPB	chr2:183744875-183744924	HepG2	liver:	n/a	chr2:183744900-183744911
48	CEBPB	chr2:183762393-183762525	A549	lung:	n/a	n/a
49	CEBPB	chr2:183756418-183756675	Hela-S3	cervix:	n/a	chr2:183756554-183756567 chr2:183756555-183756566 chr2:183756554-183756567
50	CEBPB	chr2:183679659-183679922	HepG2	liver:	n/a	chr2:183679810-183679823 chr2:183679811-183679822

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183730940-183730990	Hepatocyte	liver:	n/a
2	chr2:183730940-183730990	Hepatocyte	liver:	n/a
3	chr2:183731944-183731994	ovcar-3	ovarian:	n/a
4	chr2:183683268-183683318	U87	brain:	n/a
5	chr2:183683268-183683318	GM12878	blood:	n/a
6	chr2:183699153-183699203	HCF	heart:	n/a
7	chr2:183731824-183731874	GM12878	blood:	n/a
8	chr2:183723096-183723146	U87	brain:	n/a
9	chr2:183731407-183731457	ProgFib	skin:	n/a
10	chr2:183732607-183732657	HCT-116	colon:	n/a
11	chr2:183683268-183683318	AoSMC	blood vessel:	n/a
12	chr2:183731407-183731457	CMK	blood:	n/a
13	chr2:183731676-183731726	K562	blood:	n/a
14	chr2:183731169-183731219	HUVEC	blood vessel:	n/a
15	chr2:183732607-183732657	GM12892	blood:	n/a
16	chr2:183723096-183723146	IMR90	lung:	fetal
17	chr2:183732607-183732657	H1-hESC	embryonic stem cell:	embryo
18	chr2:183731563-183731613	GM06990	blood:	n/a
19	chr2:183731310-183731360	Hela-S3	cervix:	n/a
20	chr2:183731563-183731613	A549	lung:	n/a
21	chr2:183732062-183732112	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:183732607-183732657	SK-N-MC	brain:	n/a
23	chr2:183730940-183730990	GM12878	blood:	n/a
24	chr2:183732607-183732657	T-47D	breast:	n/a
25	chr2:183731944-183731994	MCF-7	breast:	n/a
26	chr2:183667124-183667174	NB4	blood:	n/a
27	chr2:183731824-183731874	HNPCEpiC	eye:	n/a
28	chr2:183732607-183732657	HEEpiC	esophagus:	n/a
29	chr2:183731310-183731360	A549	lung:	n/a
30	chr2:183733105-183733155	H1-hESC	embryonic stem cell:	embryo
31	chr2:183733105-183733155	HRE	kidney:	n/a
32	chr2:183667124-183667174	ProgFib	skin:	n/a
33	chr2:183731169-183731219	AG10803	skin:	n/a
34	chr2:183731599-183731649	AG04449	skin:	fetal
35	chr2:183731832-183731882	AG09309	skin:	n/a
36	chr2:183731676-183731726	PrEC	prostate:	n/a
37	chr2:183731169-183731219	GM12891	blood:	n/a
38	chr2:183731599-183731649	AoSMC	blood vessel:	n/a
39	chr2:183731944-183731994	Jurkat	blood:	n/a
40	chr2:183719355-183719405	HMEC	breast:	n/a
41	chr2:183731310-183731360	HL-60	blood:	n/a
42	chr2:183731824-183731874	U87	brain:	n/a
43	chr2:183732607-183732657	ProgFib	skin:	n/a
44	chr2:183731310-183731360	BJ	skin:	n/a
45	chr2:183731832-183731882	Caco-2	colon:	n/a
46	chr2:183730940-183730990	HCM	heart:	n/a
47	chr2:183667124-183667174	HPAEpiC	pulmonary alveolar:	n/a
48	chr2:183732062-183732112	HepG2	liver:	n/a
49	chr2:183683268-183683318	HCT-116	colon:	n/a
50	chr2:183719355-183719405	A549	lung:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:183706094..183709034-chr2:183715040..183717717,2	K562	blood:
2	chr2:183775532..183777640-chr2:183990491..183993127,2	K562	blood:
3	chr2:183750442..183752210-chr2:183755879..183757846,2	K562	blood:
4	chr2:183648162..183650730-chr2:183663988..183666770,2	K562	blood:
5	chr2:183764300..183766706-chr2:183778634..183780515,2	MCF-7	breast:
6	chr2:183695751..183697908-chr2:183701079..183703543,2	K562	blood:
7	chr2:183703011..183705323-chr2:183709490..183712980,3	K562	blood:
8	chr2:183691013..183692579-chr2:183710091..183711908,2	MCF-7	breast:
9	chr2:183750442..183752210-chr2:183755879..183757846,2	K562	blood:
10	chr2:183771103..183773642-chr2:183778453..183781754,3	K562	blood:
11	chr2:183706383..183709007-chr2:183718084..183719976,2	K562	blood:
12	chr2:183664890..183667245-chr2:183673485..183675403,2	K562	blood:
13	chr2:183695751..183697908-chr2:183701079..183703543,2	K562	blood:
14	chr2:183686694..183689194-chr2:183689476..183692268,2	K562	blood:
15	chr2:183736856..183738517-chr2:183740289..183742919,2	MCF-7	breast:
16	chr2:183759211..183762247-chr2:183762468..183766311,3	K562	blood:
17	chr2:183664890..183667245-chr2:183673485..183675403,2	K562	blood:
18	chr2:183691773..183694607-chr2:183701839..183703890,2	K562	blood:
19	chr2:183752548..183754823-chr2:183756546..183759081,2	K562	blood:
20	chr2:183666474..183669367-chr2:183675559..183677309,2	K562	blood:
21	chr2:183706094..183709034-chr2:183715040..183717717,2	K562	blood:
22	chr2:183736856..183738517-chr2:183740289..183742919,2	MCF-7	breast:
23	chr2:183759211..183762247-chr2:183762468..183766311,3	K562	blood:
24	chr2:183676835..183678660-chr2:183680847..183683198,2	K562	blood:
25	chr2:183666072..183668811-chr2:183672766..183675135,2	MCF-7	breast:
26	chr2:183676835..183678660-chr2:183680847..183683198,2	K562	blood:
27	chr2:183705476..183706982-chr2:183723282..183724982,2	K562	blood:
28	chr2:183757338..183762208-chr2:183763229..183766079,6	K562	blood:
29	chr2:183765609..183768304-chr2:183794647..183796212,2	K562	blood:
30	chr2:183758074..183761061-chr2:183762442..183764748,3	MCF-7	breast:
31	chr2:183722339..183724841-chr2:183796407..183799303,2	K562	blood:
32	chr2:183700483..183702944-chr2:183767110..183769629,2	K562	blood:
33	chr2:183767158..183769431-chr2:183778659..183782092,3	K562	blood:
34	chr2:183605695..183607908-chr2:183711047..183713446,2	K562	blood:
35	chr2:183757338..183762208-chr2:183763229..183766079,6	K562	blood:
36	chr2:183649264..183650285-chr2:183734657..183735584,4	MCF-7	breast:
37	chr2:183773913..183775803-chr2:183777634..183779722,2	K562	blood:
38	chr2:183668592..183670850-chr2:183672599..183674882,2	K562	blood:
39	chr2:183758074..183761061-chr2:183762442..183764748,3	MCF-7	breast:
40	chr2:183700483..183702944-chr2:183767110..183769629,2	K562	blood:
41	chr2:183660311..183663383-chr2:183663723..183666825,3	K562	blood:
42	chr2:183706383..183709007-chr2:183718084..183719976,2	K562	blood:
43	chr2:183686694..183689194-chr2:183689476..183692268,2	K562	blood:
44	chr2:183691013..183692579-chr2:183710091..183711908,2	MCF-7	breast:
45	chr2:183752548..183754823-chr2:183756546..183759081,2	K562	blood:
46	chr2:183705476..183706982-chr2:183723282..183724982,2	K562	blood:
47	chr2:183676117..183678247-chr2:183702144..183703855,2	MCF-7	breast:
48	chr2:183666072..183668811-chr2:183672766..183675135,2	MCF-7	breast:
49	chr2:183659213..183661128-chr2:183664377..183666463,2	MCF-7	breast:
50	chr2:183668592..183670850-chr2:183672599..183674882,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NCKAP1-2	chr2:183774745-183774992	NONHSAT075924

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FRZB	hsa-miR-30b-5p	chr2:183699473-183699467
2	FRZB	hsa-miR-30b-5p	chr2:183699080-183699101
3	FRZB	hsa-miR-30b-5p	chr2:183699467-183699488

Variant related genes	Relation type
FRZB	TF binding region
ENSG00000212404	TF binding region
RNU6-1122P	TF binding region
FRZB	CpG island
ENSG00000212404	CpG island
RNU6-1122P	CpG island
ENSG00000212404	chromatin interactions

Extended variants
information (count: 4013 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:4013 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180745006	chr2:183666013-183666014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs35809382	chr2:183666029-183666030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs386392016	chr2:183666030-183666031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs72898787	chr2:183666032-183666033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs578144672	chr2:183666045-183666046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543601307	chr2:183666047-183666048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534961823	chr2:183666048-183666049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573849767	chr2:183666129-183666130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542934535	chr2:183666150-183666151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184397603	chr2:183666153-183666154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4584994	chr2:183666168-183666169	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs528050140	chr2:183666227-183666228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544608489	chr2:183666234-183666235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547171987	chr2:183666294-183666295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189675923	chr2:183666300-183666301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144068176	chr2:183666329-183666330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550106404	chr2:183666355-183666356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116178820	chr2:183666356-183666357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181426013	chr2:183666367-183666368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113588404	chr2:183666376-183666377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549617543	chr2:183666382-183666383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566395593	chr2:183666466-183666467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534966970	chr2:183666483-183666484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558190598	chr2:183666572-183666573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571759581	chr2:183666574-183666575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs288343	chr2:183666593-183666594	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs556855391	chr2:183666619-183666620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573747980	chr2:183666697-183666698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542480405	chr2:183666849-183666850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186889087	chr2:183666857-183666858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145965849	chr2:183666868-183666869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537065470	chr2:183666901-183666902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189040069	chr2:183666902-183666903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564587457	chr2:183666904-183666905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs288344	chr2:183666918-183666919	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs181602154	chr2:183666919-183666920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs288345	chr2:183666932-183666933	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs148666119	chr2:183667024-183667025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186117734	chr2:183667033-183667034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs288346	chr2:183667120-183667121	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs538440898	chr2:183667124-183667125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528834881	chr2:183667146-183667147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190922914	chr2:183667196-183667197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551796110	chr2:183667207-183667208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs16823704	chr2:183667233-183667234	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs182615459	chr2:183667316-183667317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369344955	chr2:183667321-183667322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140222206	chr2:183667455-183667456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs557401090	chr2:183667519-183667520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs16823706	chr2:183667520-183667521	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Intellectual disability	22102821	CNVD
Autism	18522746	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
low-grade B-cell lymphoma tumor	18367492	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
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1290 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183665800-183667200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr2:183666200-183666400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:183666200-183667800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:183666200-183668000	Enhancers	HepG2	liver
5	chr2:183666600-183667800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr2:183666600-183668000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:183667000-183667200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:183667200-183667400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:183667200-183667800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr2:183667400-183668000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr2:183667800-183672000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr2:183668000-183668400	Weak transcription	HepG2	liver
13	chr2:183668400-183669200	Enhancers	HepG2	liver
14	chr2:183672000-183672600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr2:183672200-183672400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:183674200-183680800	Weak transcription	Right Atrium	heart
17	chr2:183675800-183676000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:183675800-183676000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:183676000-183683600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:183677200-183677600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr2:183677600-183683000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr2:183677800-183678200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr2:183678200-183681400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:183678800-183679400	Bivalent Enhancer	HepG2	liver
25	chr2:183679400-183679600	Flanking Bivalent TSS/Enh	HepG2	liver
26	chr2:183679600-183680000	Flanking Active TSS	HepG2	liver
27	chr2:183680000-183682400	Enhancers	HepG2	liver
28	chr2:183681400-183682400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr2:183681400-183682400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr2:183681400-183682400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr2:183681400-183682400	Enhancers	HSMMtube	muscle
32	chr2:183681400-183682400	Enhancers	NHDF-Ad	bronchial
33	chr2:183681400-183683200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr2:183681400-183683400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr2:183681400-183683400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:183681400-183683400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr2:183681400-183683800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr2:183681400-183684000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr2:183681400-183684200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr2:183681600-183682000	Enhancers	Rectal Smooth Muscle	rectum
41	chr2:183681600-183682200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr2:183681600-183682200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr2:183681600-183682200	Enhancers	NHLF	lung
44	chr2:183681600-183682400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr2:183681600-183682400	Enhancers	Fetal Heart	heart
46	chr2:183681600-183682400	Enhancers	Fetal Lung	lung
47	chr2:183681600-183682600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr2:183681600-183682600	Enhancers	HSMM	muscle
49	chr2:183681600-183682800	Enhancers	Fetal Stomach	stomach
50	chr2:183681600-183683400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links