Variant report

Variant	nsv522138
Chromosome Location	chr4:22878904-23002014
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	ARID3A	chr4:22971300-22971641	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:22897036-22897520	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:22899272-22899454	K562	blood:	n/a	n/a
4	ARID3A	chr4:22899185-22899471	HepG2	liver:	n/a	n/a
5	BACH1	chr4:22999486-22999794	K562	blood:	n/a	n/a
6	BACH1	chr4:22918677-22918719	K562	blood:	n/a	n/a
7	BATF	chr4:22935474-22935715	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:22885743-22886105	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr4:22935500-22935722	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:22935546-22935707	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:22885970-22886163	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr4:22999060-22999284	K562	blood:	n/a	n/a
13	BHLHE40	chr4:22896975-22897295	HepG2	liver:	n/a	n/a
14	BRCA1	chr4:22899347-22899433	HepG2	liver:	n/a	n/a
15	CCNT2	chr4:22990380-22990846	K562	blood:	n/a	n/a
16	CEBPB	chr4:22970778-22971746	A549	lung:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
17	CEBPB	chr4:22885915-22886185	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:22971200-22971684	A549	lung:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
19	CEBPB	chr4:23001185-23001413	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:22981018-22981257	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:22962760-22963052	IMR90	lung:	n/a	chr4:22962918-22962931 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962918-22962931
22	CEBPB	chr4:22971259-22971582	MCF-7	breast:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
23	CEBPB	chr4:22919748-22920078	HepG2	liver:	n/a	chr4:22919913-22919924 chr4:22919915-22919924 chr4:22919913-22919926 chr4:22919914-22919925
24	CEBPB	chr4:22970866-22971624	HepG2	liver:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
25	CEBPB	chr4:22980955-22981301	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:22919827-22920036	A549	lung:	n/a	chr4:22919913-22919924 chr4:22919915-22919924 chr4:22919913-22919926 chr4:22919914-22919925
27	CEBPB	chr4:22970806-22971591	IMR90	lung:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
28	CEBPB	chr4:22919828-22920030	IMR90	lung:	n/a	chr4:22919913-22919924 chr4:22919915-22919924 chr4:22919913-22919926 chr4:22919914-22919925
29	CEBPB	chr4:22937900-22938162	HepG2	liver:	n/a	chr4:22938010-22938021
30	CEBPB	chr4:22980982-22981263	K562	blood:	n/a	n/a
31	CEBPB	chr4:22962790-22963068	K562	blood:	n/a	chr4:22962918-22962931 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962918-22962931
32	CEBPB	chr4:22962748-22963083	HepG2	liver:	n/a	chr4:22962918-22962931 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962918-22962931
33	CEBPB	chr4:22924888-22925085	A549	lung:	n/a	chr4:22925064-22925075
34	CEBPB	chr4:22924952-22925152	HepG2	liver:	n/a	chr4:22925064-22925075
35	CEBPB	chr4:22980980-22981287	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:22970806-22971153	A549	lung:	n/a	n/a
37	CEBPB	chr4:22970760-22971748	Hela-S3	cervix:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
38	CEBPB	chr4:22970805-22971583	A549	lung:	n/a	chr4:22971420-22971433 chr4:22971420-22971431 chr4:22971422-22971433
39	CEBPB	chr4:22962805-22963050	A549	lung:	n/a	chr4:22962918-22962931 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962920-22962929 chr4:22962918-22962931
40	CHD2	chr4:22885793-22886098	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr4:22998899-22999324	K562	blood:	n/a	n/a
42	CHD2	chr4:22907991-22908003	GM12878	blood:	n/a	n/a
43	CTCF	chr4:22899300-22899450	HCM	heart:	n/a	chr4:22899320-22899329 chr4:22899320-22899333 chr4:22899318-22899334 chr4:22899319-22899340 chr4:22899317-22899335
44	CTCF	chr4:23001180-23001330	HepG2	liver:	n/a	n/a
45	CTCF	chr4:22899304-22899450	Fibrobl	skin:	n/a	chr4:22899320-22899329 chr4:22899320-22899333 chr4:22899318-22899334 chr4:22899319-22899340 chr4:22899317-22899335
46	CTCF	chr4:22964140-22964290	AoAF	blood vessel:	n/a	chr4:22964210-22964228 chr4:22964212-22964233
47	CTCF	chr4:22899346-22899396	GM19239	blood:	n/a	n/a
48	CTCF	chr4:22899220-22899370	HUVEC	blood vessel:	n/a	chr4:22899320-22899329 chr4:22899320-22899333 chr4:22899318-22899334 chr4:22899319-22899340 chr4:22899317-22899335
49	CTCF	chr4:22964240-22964390	AG04450	lung:	n/a	n/a
50	CTCF	chr4:22964160-22964310	GM12864	blood:	n/a	chr4:22964210-22964228 chr4:22964212-22964233

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:22998088-22998138	AG04450	lung:	fetal
2	chr4:22913868-22913918	MCF-7	breast:	n/a
3	chr4:22913868-22913918	ovcar-3	ovarian:	n/a
4	chr4:22913868-22913918	SK-N-SH_RA	brain:	n/a
5	chr4:22998088-22998138	SK-N-SH	brain:	n/a
6	chr4:22998088-22998138	ECC-1	luminal epithelium:	n/a
7	chr4:22999086-22999136	IMR90	lung:	fetal
8	chr4:22999086-22999136	HRCEpiC	kidney:	n/a
9	chr4:22998088-22998138	H1-hESC	embryonic stem cell:	embryo
10	chr4:22999077-22999127	ProgFib	skin:	n/a
11	chr4:22998088-22998138	K562	blood:	n/a
12	chr4:22999077-22999127	NH-A	brain:	n/a
13	chr4:22999086-22999136	HNPCEpiC	eye:	n/a
14	chr4:22913868-22913918	BJ	skin:	n/a
15	chr4:22999086-22999136	PrEC	prostate:	n/a
16	chr4:22998088-22998138	U87	brain:	n/a
17	chr4:22999077-22999127	NT2-D1	testis:	n/a
18	chr4:22998088-22998138	NH-A	brain:	n/a
19	chr4:22913868-22913918	GM06990	blood:	n/a
20	chr4:22913868-22913918	SKMC	muscle:	n/a
21	chr4:22999077-22999127	HNPCEpiC	eye:	n/a
22	chr4:22999077-22999127	HL-60	blood:	n/a
23	chr4:22999077-22999127	SK-N-MC	brain:	n/a
24	chr4:22999086-22999136	HEK293	kidney:	embryo
25	chr4:22999077-22999127	HCPEpiC	choroid plexus:	n/a
26	chr4:22999086-22999136	AoSMC	blood vessel:	n/a
27	chr4:22998088-22998138	SAEC	small airway:	n/a
28	chr4:22913868-22913918	CMK	blood:	n/a
29	chr4:22913868-22913918	SK-N-SH	brain:	n/a
30	chr4:22998088-22998138	NHBE	bronchial:	n/a
31	chr4:22913868-22913918	MCF10A-Er-Src	breast:	n/a
32	chr4:22999086-22999136	HIPEpiC	eye:	n/a
33	chr4:22999077-22999127	AoSMC	blood vessel:	n/a
34	chr4:22999086-22999136	AG04449	skin:	fetal
35	chr4:22913868-22913918	HEEpiC	esophagus:	n/a
36	chr4:22999086-22999136	NH-A	brain:	n/a
37	chr4:22999077-22999127	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:22913868-22913918	HCT-116	colon:	n/a
39	chr4:22999086-22999136	HepG2	liver:	n/a
40	chr4:22999077-22999127	MCF-7	breast:	n/a
41	chr4:22913868-22913918	HEK293	kidney:	embryo
42	chr4:22999077-22999127	NHDF-neo	bronchial:	n/a
43	chr4:22999077-22999127	AG09309	skin:	n/a
44	chr4:22998088-22998138	IMR90	lung:	fetal
45	chr4:22999077-22999127	A549	lung:	n/a
46	chr4:22913868-22913918	NH-A	brain:	n/a
47	chr4:22998088-22998138	HUVEC	blood vessel:	n/a
48	chr4:22999086-22999136	SK-N-MC	brain:	n/a
49	chr4:22999086-22999136	SKMC	muscle:	n/a
50	chr4:22999086-22999136	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:22875811..22877491-chr4:22882089..22884830,2	K562	blood:
2	chr4:22998275..23001273-chr4:23003016..23005403,4	K562	blood:
3	chr4:22927818..22930601-chr4:22932236..22933827,2	K562	blood:
4	chr4:22899142..22899801-chr4:24420786..24421361,2	MCF-7	breast:
5	chr4:22938501..22940847-chr4:22943530..22945759,2	K562	blood:
6	chr4:22927818..22930601-chr4:22932236..22933827,2	K562	blood:
7	chr4:22992595..22995283-chr4:22996612..22998977,2	K562	blood:
8	chr4:22992595..22995283-chr4:22996612..22998977,2	K562	blood:
9	chr4:22938501..22940847-chr4:22943530..22945759,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SOD3-6	chr4:22999174-22999236	ENSG00000248837
2	lnc-SOD3-6	chr4:23001208-23001335	ENSG00000248837
3	lnc-SOD3-6	chr4:22999105-22999236	NONHSAT095769
4	lnc-SOD3-6	chr4:23001208-23001335	NONHSAT095769
5	lnc-SOD3-6	chr4:23001209-23001335	ENSG00000248837

Variant related genes	Relation type
ENSG00000248837	TF binding region
ENSG00000248837	CpG island
ENSG00000248837	chromatin interactions
MYH4	miRNA target sites
SRGAP1	miRNA target sites

Extended variants
information (count: 2304 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2304 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6840245	chr4:22878904-22878905	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532628408	chr4:22878930-22878931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7683022	chr4:22878986-22878987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544017759	chr4:22879006-22879007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373897232	chr4:22879025-22879026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564901	chr4:22879039-22879040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs590020	chr4:22879042-22879043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77961099	chr4:22879054-22879055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188171025	chr4:22879061-22879062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11722687	chr4:22879079-22879080	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs559370392	chr4:22879083-22879084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142304541	chr4:22879086-22879087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551423952	chr4:22879114-22879115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151304442	chr4:22879118-22879119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11734884	chr4:22879126-22879127	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs550143922	chr4:22879166-22879167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs114536916	chr4:22879202-22879203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79491467	chr4:22879222-22879223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534956005	chr4:22879223-22879224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191392024	chr4:22879237-22879238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577664534	chr4:22879243-22879244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558797096	chr4:22879256-22879257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529695472	chr4:22879257-22879258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557057103	chr4:22879289-22879290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575441456	chr4:22879409-22879410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565905538	chr4:22879427-22879428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79000704	chr4:22879428-22879429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183165794	chr4:22879475-22879476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187454645	chr4:22879502-22879503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192559848	chr4:22879531-22879532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs424020	chr4:22879549-22879550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569283134	chr4:22879573-22879574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534892422	chr4:22879578-22879579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76065865	chr4:22879585-22879586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533123908	chr4:22879668-22879669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115368263	chr4:22879674-22879675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563417729	chr4:22879687-22879688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367745897	chr4:22879742-22879743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531066305	chr4:22879774-22879775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140055785	chr4:22879801-22879802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115972232	chr4:22879850-22879851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs16873199	chr4:22879857-22879858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546874642	chr4:22879956-22879957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184744332	chr4:22880000-22880001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200251242	chr4:22880100-22880101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186799801	chr4:22880128-22880129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192502695	chr4:22880141-22880142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372789240	chr4:22880188-22880189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536394495	chr4:22880237-22880238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184430412	chr4:22880259-22880260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22874800-22879000	Enhancers	Fetal Intestine Large	intestine
2	chr4:22878600-22880800	Enhancers	Brain Germinal Matrix	brain
3	chr4:22878800-22879600	Enhancers	Fetal Brain Female	brain
4	chr4:22878800-22881200	Weak transcription	Fetal Intestine Small	intestine
5	chr4:22879000-22880200	Weak transcription	Fetal Intestine Large	intestine
6	chr4:22880600-22880800	Enhancers	Fetal Intestine Large	intestine
7	chr4:22881200-22881400	Enhancers	Fetal Intestine Small	intestine
8	chr4:22883200-22883800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:22884000-22887400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:22886800-22887600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr4:22896400-22899200	Enhancers	HepG2	liver
12	chr4:22896800-22898000	Enhancers	Liver	Liver
13	chr4:22898200-22899000	Enhancers	Fetal Lung	lung
14	chr4:22898600-22899200	Enhancers	Fetal Intestine Small	intestine
15	chr4:22899000-22902400	Weak transcription	Fetal Lung	lung
16	chr4:22899400-22901000	Enhancers	Primary hematopoietic stem cells	blood
17	chr4:22899400-22901200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr4:22900000-22901200	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr4:22900000-22901200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr4:22900400-22900800	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr4:22901200-22905200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr4:22902200-22903000	Enhancers	Colon Smooth Muscle	Colon
23	chr4:22902400-22903000	Enhancers	Fetal Lung	lung
24	chr4:22902600-22903000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr4:22902800-22903200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:22903000-22903600	Weak transcription	Fetal Lung	lung
27	chr4:22903200-22903400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:22903400-22903800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:22903600-22903800	Enhancers	Fetal Lung	lung
30	chr4:22903600-22904200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:22905200-22905800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr4:22905200-22906000	Enhancers	Fetal Heart	heart
33	chr4:22905800-22906000	Enhancers	Duodenum Mucosa	Duodenum
34	chr4:22906000-22906800	Weak transcription	Duodenum Mucosa	Duodenum
35	chr4:22906400-22908400	Enhancers	Fetal Intestine Small	intestine
36	chr4:22906800-22908200	Enhancers	Duodenum Mucosa	Duodenum
37	chr4:22907200-22907600	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr4:22907200-22908200	Enhancers	Fetal Intestine Large	intestine
39	chr4:22907800-22908200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:22911600-22913000	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr4:22912000-22912400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr4:22912000-22914200	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr4:22913000-22914000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr4:22913200-22913800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:22913200-22914200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:22913400-22914000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr4:22913400-22914200	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr4:22913600-22914200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:22914000-22914200	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr4:22914200-22915200	Weak transcription	Primary monocytes fromperipheralblood	blood

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