Variant report

Variant	nsv875484
Chromosome Location	chr2:183702964-183747442
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:407)
CpG islands
(count:979)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:183731010-183731021	HepG2	liver:	n/a	n/a
2	ATF1	chr2:183725934-183726010	K562	blood:	n/a	n/a
3	BACH1	chr2:183732098-183732408	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:183730971-183731063	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr2:183735041-183735273	K562	blood:	n/a	n/a
6	BRCA1	chr2:183732940-183733129	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr2:183731451-183731729	HepG2	liver:	n/a	n/a
8	CCNT2	chr2:183735166-183735220	K562	blood:	n/a	n/a
9	CEBPB	chr2:183731324-183731676	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:183726801-183727122	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:183741611-183741653	HepG2	liver:	n/a	chr2:183741618-183741629
12	CEBPB	chr2:183731437-183731586	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:183731254-183731648	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:183732886-183733095	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:183744875-183744924	HepG2	liver:	n/a	chr2:183744900-183744911
16	CEBPB	chr2:183734241-183734433	HepG2	liver:	n/a	chr2:183734351-183734362
17	CEBPB	chr2:183726813-183727013	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPZ	chr2:183731571-183731646	HepG2	liver:	n/a	n/a
19	CHD2	chr2:183731102-183731106	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTBP2	chr2:183730793-183732591	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr2:183732200-183732350	GM12864	blood:	n/a	n/a
22	CTCF	chr2:183735040-183735190	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr2:183735000-183735150	GM12873	blood:	n/a	n/a
24	CTCF	chr2:183727485-183727647	MCF-7	breast:	n/a	n/a
25	CTCF	chr2:183735047-183735220	GM12891	blood:	n/a	n/a
26	CTCF	chr2:183734980-183735130	HMF	breast:	n/a	n/a
27	CTCF	chr2:183735060-183735210	HEK293	kidney:	n/a	n/a
28	CTCF	chr2:183731840-183731990	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr2:183735012-183735249	NHEK	skin:	n/a	n/a
30	CTCF	chr2:183735060-183735210	GM12874	blood:	n/a	n/a
31	CTCF	chr2:183735100-183735250	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr2:183731880-183732030	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr2:183735059-183735212	ProgFib	skin:	n/a	n/a
34	CTCF	chr2:183734999-183735270	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:183727547-183727607	NHEK	skin:	n/a	n/a
36	CTCF	chr2:183735024-183735251	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr2:183734960-183735110	HMEC	breast:	n/a	n/a
38	CTCF	chr2:183735047-183735213	GM10266	blood:	n/a	n/a
39	CTCF	chr2:183735100-183735250	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr2:183734980-183735130	HFF	foreskin:	n/a	n/a
41	CTCF	chr2:183735040-183735190	HRE	kidney:	n/a	n/a
42	CTCF	chr2:183734980-183735130	GM06990	blood:	n/a	n/a
43	CTCF	chr2:183735038-183735223	GM12892	blood:	n/a	n/a
44	CTCF	chr2:183735080-183735230	AG04449	skin:	n/a	n/a
45	CTCF	chr2:183727460-183727610	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr2:183727500-183727650	GM12870	blood:	n/a	n/a
47	CTCF	chr2:183734920-183735070	HCM	heart:	n/a	n/a
48	CTCF	chr2:183731240-183731390	AG04449	skin:	n/a	n/a
49	CTCF	chr2:183735040-183735190	GM12864	blood:	n/a	n/a
50	CTCF	chr2:183735017-183735248	Gliobla	brain:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183731169-183731219	LNCaP	prostate:	n/a
2	chr2:183732607-183732657	NHBE	bronchial:	n/a
3	chr2:183731832-183731882	U87	brain:	n/a
4	chr2:183731169-183731219	LNCaP	prostate:	n/a
5	chr2:183732607-183732657	NHBE	bronchial:	n/a
6	chr2:183731832-183731882	U87	brain:	n/a
7	chr2:183731832-183731882	HRE	kidney:	n/a
8	chr2:183729189-183729239	MCF10A-Er-Src	breast:	n/a
9	chr2:183719355-183719405	ProgFib	skin:	n/a
10	chr2:183731407-183731457	GM06990	blood:	n/a
11	chr2:183730940-183730990	HNPCEpiC	eye:	n/a
12	chr2:183730940-183730990	NHBE	bronchial:	n/a
13	chr2:183731824-183731874	HepG2	liver:	n/a
14	chr2:183731169-183731219	A549	lung:	n/a
15	chr2:183731824-183731874	AG10803	skin:	n/a
16	chr2:183733105-183733155	NT2-D1	testis:	n/a
17	chr2:183729189-183729239	HCF	heart:	n/a
18	chr2:183731944-183731994	BE2_C	brain:	n/a
19	chr2:183731676-183731726	GM12891	blood:	n/a
20	chr2:183731824-183731874	HRPEpiC	eye:	n/a
21	chr2:183731824-183731874	MCF10A-Er-Src	breast:	n/a
22	chr2:183733105-183733155	CMK	blood:	n/a
23	chr2:183731563-183731613	GM12891	blood:	n/a
24	chr2:183731824-183731874	RPTEC	kidney:	n/a
25	chr2:183731407-183731457	LNCaP	prostate:	n/a
26	chr2:183733105-183733155	HCT-116	colon:	n/a
27	chr2:183723096-183723146	HCPEpiC	choroid plexus:	n/a
28	chr2:183730940-183730990	BJ	skin:	n/a
29	chr2:183733105-183733155	SK-N-SH_RA	brain:	n/a
30	chr2:183731407-183731457	AG10803	skin:	n/a
31	chr2:183731310-183731360	AG09319	gingival:	n/a
32	chr2:183731944-183731994	GM12891	blood:	n/a
33	chr2:183723096-183723146	MCF-7	breast:	n/a
34	chr2:183731407-183731457	HCM	heart:	n/a
35	chr2:183731832-183731882	HepG2	liver:	n/a
36	chr2:183730940-183730990	Jurkat	blood:	n/a
37	chr2:183731599-183731649	GM19239	blood:	n/a
38	chr2:183731563-183731613	HUVEC	blood vessel:	n/a
39	chr2:183732607-183732657	GM12891	blood:	n/a
40	chr2:183731407-183731457	NH-A	brain:	n/a
41	chr2:183723096-183723146	SK-N-SH	brain:	n/a
42	chr2:183731563-183731613	AG10803	skin:	n/a
43	chr2:183731563-183731613	HRPEpiC	eye:	n/a
44	chr2:183731407-183731457	MCF10A-Er-Src	breast:	n/a
45	chr2:183733105-183733155	IMR90	lung:	fetal
46	chr2:183719355-183719405	HepG2	liver:	n/a
47	chr2:183723096-183723146	Hepatocyte	liver:	n/a
48	chr2:183732607-183732657	HRE	kidney:	n/a
49	chr2:183731599-183731649	GM12878	blood:	n/a
50	chr2:183730940-183730990	PFSK-1	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:183705476..183706982-chr2:183723282..183724982,2	K562	blood:
2	chr2:183706094..183709034-chr2:183715040..183717717,2	K562	blood:
3	chr2:183703011..183705323-chr2:183709490..183712980,3	K562	blood:
4	chr2:183736856..183738517-chr2:183740289..183742919,2	MCF-7	breast:
5	chr2:183706383..183709007-chr2:183718084..183719976,2	K562	blood:
6	chr2:183705476..183706982-chr2:183723282..183724982,2	K562	blood:
7	chr2:183649264..183650285-chr2:183734657..183735584,4	MCF-7	breast:
8	chr2:183695751..183697908-chr2:183701079..183703543,2	K562	blood:
9	chr2:183703011..183705323-chr2:183709490..183712980,3	K562	blood:
10	chr2:183676117..183678247-chr2:183702144..183703855,2	MCF-7	breast:
11	chr2:183736856..183738517-chr2:183740289..183742919,2	MCF-7	breast:
12	chr2:183605695..183607908-chr2:183711047..183713446,2	K562	blood:
13	chr2:183691013..183692579-chr2:183710091..183711908,2	MCF-7	breast:
14	chr2:183691773..183694607-chr2:183701839..183703890,2	K562	blood:
15	chr2:183706094..183709034-chr2:183715040..183717717,2	K562	blood:
16	chr2:183706383..183709007-chr2:183718084..183719976,2	K562	blood:
17	chr2:183722339..183724841-chr2:183796407..183799303,2	K562	blood:

No data

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

Extended variants
information (count: 1617 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1617 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1561369	chr2:183702964-183702965	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566297178	chr2:183702997-183702998	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574542486	chr2:183703046-183703047	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs535275347	chr2:183703054-183703055	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs558175479	chr2:183703055-183703056	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs180673879	chr2:183703056-183703057	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375931244	chr2:183703068-183703069	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs200080125	chr2:183703120-183703121	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs374178563	chr2:183703130-183703131	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs141551747	chr2:183703143-183703144	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs185490352	chr2:183703144-183703145	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs138147194	chr2:183703147-183703148	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139802041	chr2:183703181-183703182	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs370385346	chr2:183703208-183703209	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374712103	chr2:183703221-183703222	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs367887067	chr2:183703227-183703228	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs143282639	chr2:183703229-183703230	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs112797950	chr2:183703239-183703240	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs572705327	chr2:183703240-183703241	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs371741810	chr2:183703257-183703258	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200889851	chr2:183703312-183703313	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs288326	chr2:183703336-183703337	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs369134765	chr2:183703367-183703368	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565076041	chr2:183703407-183703408	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372841486	chr2:183703416-183703417	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530527579	chr2:183703426-183703427	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377391568	chr2:183703455-183703456	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs558179983	chr2:183703524-183703525	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs181382567	chr2:183703534-183703535	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370683775	chr2:183703540-183703541	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs2840042	chr2:183703655-183703656	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546719691	chr2:183703686-183703687	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373508829	chr2:183703694-183703695	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115520755	chr2:183703703-183703704	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs565547293	chr2:183703728-183703729	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377268067	chr2:183703731-183703732	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552047073	chr2:183703779-183703780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571874719	chr2:183703785-183703786	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs143311507	chr2:183703791-183703792	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs146200681	chr2:183703813-183703814	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs573720382	chr2:183703836-183703837	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs186006508	chr2:183703864-183703865	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs553061899	chr2:183703942-183703943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572986829	chr2:183704013-183704014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544923903	chr2:183704014-183704015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565168381	chr2:183704015-183704016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575411595	chr2:183704038-183704039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544538172	chr2:183704049-183704050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12611837	chr2:183704084-183704085	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs139307427	chr2:183704104-183704105	Enhancers Weak transcription	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
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:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183689800-183719200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:183691800-183704800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr2:183692200-183704600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr2:183693200-183705200	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr2:183697600-183703000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:183697800-183704600	Weak transcription	Aorta	Aorta
7	chr2:183701600-183704200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr2:183701600-183704600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:183701800-183703600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:183702000-183704200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr2:183702200-183704200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr2:183702400-183703800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr2:183702400-183711200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr2:183702600-183716800	Weak transcription	HSMMtube	muscle
15	chr2:183703000-183703400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:183703200-183704000	Enhancers	Fetal Intestine Large	intestine
17	chr2:183703400-183703600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:183703400-183704800	Enhancers	Fetal Heart	heart
19	chr2:183703600-183705000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:183703600-183705400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:183703800-183704000	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr2:183703800-183704200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:183704000-183710000	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr2:183704200-183705000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr2:183704200-183705000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr2:183704200-183706800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr2:183704400-183704600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr2:183704400-183705000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr2:183704400-183705200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:183704600-183704800	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr2:183704600-183705000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:183704600-183705000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr2:183704600-183705000	Active TSS	Aorta	Aorta
34	chr2:183704800-183705000	Enhancers	Stomach Smooth Muscle	stomach
35	chr2:183705000-183705200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
36	chr2:183705000-183705400	Weak transcription	Stomach Smooth Muscle	stomach
37	chr2:183705000-183706400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:183705000-183710400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:183705000-183716600	Weak transcription	Aorta	Aorta
40	chr2:183705200-183706600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr2:183705200-183710400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr2:183705400-183705600	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr2:183705400-183705600	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr2:183705400-183705600	Enhancers	Stomach Smooth Muscle	stomach
45	chr2:183705600-183710400	Weak transcription	Stomach Smooth Muscle	stomach
46	chr2:183706400-183707800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:183706600-183707200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr2:183706800-183707200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:183707200-183708400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr2:183707800-183709800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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