Variant report

Variant	nsv830785
Chromosome Location	chr6:117448943-117627275
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:942)
CpG islands
(count:1710)
Chromatin interactive
region (count:10)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:942 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:117548019-117548316	HepG2	liver:	n/a	n/a
2	ATF2	chr6:117586060-117586371	GM12878	blood:	n/a	n/a
3	BACH1	chr6:117592194-117592308	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:117586712-117586778	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:117591194-117591325	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:117593759-117594104	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:117459342-117459361	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr6:117561663-117561856	GM12878	blood:	n/a	n/a
9	CBX3	chr6:117488717-117489231	HCT-116	colon:	n/a	n/a
10	CCNT2	chr6:117538241-117538436	K562	blood:	n/a	n/a
11	CCNT2	chr6:117476295-117476440	K562	blood:	n/a	n/a
12	CCNT2	chr6:117620327-117620446	K562	blood:	n/a	n/a
13	CEBPB	chr6:117554489-117554800	HepG2	liver:	n/a	chr6:117554655-117554666
14	CEBPB	chr6:117516940-117517351	HCT-116	colon:	n/a	chr6:117517085-117517096
15	CEBPB	chr6:117516918-117517266	Hela-S3	cervix:	n/a	chr6:117517085-117517096
16	CEBPB	chr6:117516923-117517217	HepG2	liver:	n/a	chr6:117517085-117517096
17	CEBPB	chr6:117548007-117548706	HepG2	liver:	n/a	chr6:117548497-117548508 chr6:117548495-117548506
18	CEBPB	chr6:117550047-117550129	A549	lung:	n/a	chr6:117550075-117550086
19	CEBPB	chr6:117587004-117587185	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr6:117549961-117550163	HepG2	liver:	n/a	chr6:117550075-117550086
21	CEBPB	chr6:117560505-117560830	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:117601351-117601551	HepG2	liver:	n/a	chr6:117601467-117601478
23	CEBPB	chr6:117591356-117591416	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr6:117516938-117517254	H1-hESC	embryonic stem cell:	n/a	chr6:117517085-117517096
25	CEBPB	chr6:117486492-117486632	HepG2	liver:	n/a	chr6:117486549-117486560 chr6:117486549-117486562 chr6:117486551-117486562
26	CEBPB	chr6:117554591-117554700	A549	lung:	n/a	chr6:117554655-117554666
27	CEBPB	chr6:117516814-117517281	HCT-116	colon:	n/a	chr6:117517085-117517096
28	CHD1	chr6:117592127-117592222	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr6:117591181-117591739	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr6:117591297-117591320	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr6:117603480-117603676	K562	blood:	n/a	n/a
32	CHD2	chr6:117586262-117586360	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr6:117586600-117587155	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTBP2	chr6:117591168-117592322	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTBP2	chr6:117585407-117586358	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTBP2	chr6:117586727-117587425	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr6:117510140-117510290	GM12875	blood:	n/a	chr6:117510166-117510184
38	CTCF	chr6:117602200-117602350	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr6:117488840-117488990	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr6:117488800-117488950	HL-60	blood:	n/a	n/a
41	CTCF	chr6:117602220-117602370	GM12872	blood:	n/a	n/a
42	CTCF	chr6:117480200-117480350	HepG2	liver:	n/a	n/a
43	CTCF	chr6:117602174-117602396	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:117488843-117488917	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:117589420-117589570	GM12873	blood:	n/a	n/a
46	CTCF	chr6:117510120-117510270	GM12867	blood:	n/a	chr6:117510166-117510184
47	CTCF	chr6:117602180-117602330	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr6:117602110-117602403	IMR90	lung:	n/a	n/a
49	CTCF	chr6:117510100-117510250	AG09319	gingival:	n/a	chr6:117510166-117510184
50	CTCF	chr6:117586680-117586830	HPF	lung:	n/a	chr6:117586701-117586714

(count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:117584596-117584646	PANC-1	pancreas:	n/a
2	chr6:117587588-117587638	NHDF-neo	bronchial:	n/a
3	chr6:117584596-117584646	PANC-1	pancreas:	n/a
4	chr6:117587588-117587638	NHDF-neo	bronchial:	n/a
5	chr6:117584596-117584646	Jurkat	blood:	n/a
6	chr6:117591534-117591584	A549	lung:	n/a
7	chr6:117583893-117583943	Hela-S3	cervix:	n/a
8	chr6:117583181-117583231	ECC-1	luminal epithelium:	n/a
9	chr6:117584715-117584765	AG04450	lung:	fetal
10	chr6:117586681-117586731	HRCEpiC	kidney:	n/a
11	chr6:117586538-117586588	IMR90	lung:	fetal
12	chr6:117594700-117594750	HepG2	liver:	n/a
13	chr6:117591433-117591483	NB4	blood:	n/a
14	chr6:117586681-117586731	HL-60	blood:	n/a
15	chr6:117586538-117586588	ECC-1	luminal epithelium:	n/a
16	chr6:117586918-117586968	AG10803	skin:	n/a
17	chr6:117585815-117585865	A549	lung:	n/a
18	chr6:117586817-117586867	HPAEpiC	pulmonary alveolar:	n/a
19	chr6:117586593-117586643	SK-N-SH_RA	brain:	n/a
20	chr6:117584715-117584765	Caco-2	colon:	n/a
21	chr6:117586666-117586716	HMEC	breast:	n/a
22	chr6:117609650-117609700	HRE	kidney:	n/a
23	chr6:117583893-117583943	Caco-2	colon:	n/a
24	chr6:117583181-117583231	PANC-1	pancreas:	n/a
25	chr6:117592358-117592408	PrEC	prostate:	n/a
26	chr6:117585815-117585865	HCT-116	colon:	n/a
27	chr6:117585815-117585865	NHDF-neo	bronchial:	n/a
28	chr6:117592358-117592408	AG09309	skin:	n/a
29	chr6:117586817-117586867	PrEC	prostate:	n/a
30	chr6:117583181-117583231	GM12892	blood:	n/a
31	chr6:117583181-117583231	SAEC	small airway:	n/a
32	chr6:117592358-117592408	GM12891	blood:	n/a
33	chr6:117583893-117583943	HRCEpiC	kidney:	n/a
34	chr6:117586593-117586643	HepG2	liver:	n/a
35	chr6:117503272-117503322	HUVEC	blood vessel:	n/a
36	chr6:117591534-117591584	SK-N-MC	brain:	n/a
37	chr6:117583181-117583231	Jurkat	blood:	n/a
38	chr6:117583181-117583231	HAEpiC	amniotic membrane:	n/a
39	chr6:117584665-117584715	NHDF-neo	bronchial:	n/a
40	chr6:117586681-117586731	PANC-1	pancreas:	n/a
41	chr6:117586666-117586716	PrEC	prostate:	n/a
42	chr6:117584715-117584765	SAEC	small airway:	n/a
43	chr6:117592262-117592312	Jurkat	blood:	n/a
44	chr6:117584596-117584646	HRE	kidney:	n/a
45	chr6:117609650-117609700	HCT-116	colon:	n/a
46	chr6:117586225-117586275	ProgFib	skin:	n/a
47	chr6:117583893-117583943	NT2-D1	testis:	n/a
48	chr6:117585815-117585865	GM12878	blood:	n/a
49	chr6:117594700-117594750	HEK293	kidney:	embryo
50	chr6:117591433-117591483	AoSMC	blood vessel:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:117447258..117449659-chr6:117456353..117459059,2	K562	blood:
2	chr6:117290291..117290928-chr6:117516415..117517089,2	MCF-7	breast:
3	chr6:117447258..117449659-chr6:117456353..117459059,2	K562	blood:
4	chr6:117293198..117294084-chr6:117602223..117602832,3	MCF-7	breast:
5	chr6:117623559..117626369-chr6:117645253..117647045,2	K562	blood:
6	chr6:116710278..116712360-chr6:117478553..117480106,2	K562	blood:
7	chr6:117292562..117293807-chr6:117509373..117510214,3	MCF-7	breast:
8	chr6:117456061..117457595-chr6:117459840..117462446,2	K562	blood:
9	chr6:117601835..117602502-chr6:117638433..117639008,2	MCF-7	breast:
10	chr6:117456061..117457595-chr6:117459840..117462446,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VGLL2-2	chr6:117622618-117622921	NONHSAT114668
2	lnc-VGLL2-1	chr6:117620527-117620801	NONHSAT114667
3	lnc-ROS1-2	chr6:117585738-117585864	NONHSAT114666
4	lnc-ROS1-2	chr6:117583516-117584346	NONHSAT114666

No data

Variant related genes	Relation type
RN7SKP51	TF binding region
RN7SKP18	TF binding region
VGLL2	TF binding region
RN7SKP51	CpG island
RN7SKP18	CpG island
VGLL2	CpG island

Extended variants
information (count: 5098 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:5098 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145342950	chr6:117450032-117450033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs186554388	chr6:117450063-117450064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548542283	chr6:117450065-117450066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75512175	chr6:117450099-117450100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529984942	chr6:117450100-117450101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551922235	chr6:117450800-117450801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551869541	chr6:117450804-117450805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183811940	chr6:117450847-117450848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188689350	chr6:117450893-117450894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570668624	chr6:117450946-117450947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527706868	chr6:117457802-117457803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371832773	chr6:117457863-117457864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183111950	chr6:117457881-117457882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538384966	chr6:117457882-117457883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142814880	chr6:117457892-117457893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529023847	chr6:117458021-117458022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571429324	chr6:117458036-117458037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560496954	chr6:117458058-117458059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146976984	chr6:117458064-117458065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186364959	chr6:117458086-117458087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs492516	chr6:117458140-117458141	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs371891470	chr6:117458157-117458158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554589289	chr6:117458167-117458168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368464942	chr6:117458236-117458237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575943588	chr6:117458251-117458252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376536794	chr6:117458265-117458266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543508053	chr6:117458267-117458268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77663038	chr6:117458281-117458282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375167803	chr6:117458313-117458314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs72955425	chr6:117458360-117458361	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs373632683	chr6:117458405-117458406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs71989643	chr6:117458406-117458407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs151270169	chr6:117458415-117458416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs57477932	chr6:117458437-117458438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538138444	chr6:117458452-117458453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190618363	chr6:117458501-117458502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371008609	chr6:117458522-117458523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560646023	chr6:117458533-117458534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183175037	chr6:117458565-117458566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201868135	chr6:117458567-117458568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200107465	chr6:117458620-117458621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs59909212	chr6:117458621-117458622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567657098	chr6:117458674-117458675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs531569313	chr6:117458684-117458685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs514239	chr6:117458737-117458738	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs200167500	chr6:117458765-117458766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544736577	chr6:117458784-117458785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368003354	chr6:117458798-117458799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567640267	chr6:117458901-117458902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375645993	chr6:117458902-117458903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Urothelial carcinoma	21177765	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Salivary gland tumor	18059337	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Epilepsy	22083797	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1082 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117450000-117450200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr6:117450800-117451000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr6:117457800-117458000	Weak transcription	Psoas Muscle	Psoas
4	chr6:117457800-117459200	Enhancers	Left Ventricle	heart
5	chr6:117457800-117461400	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr6:117458000-117458200	Enhancers	Colon Smooth Muscle	Colon
7	chr6:117458000-117458200	Enhancers	Fetal Muscle Leg	muscle
8	chr6:117458000-117458200	Enhancers	Psoas Muscle	Psoas
9	chr6:117458000-117459000	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr6:117458200-117460200	Weak transcription	Fetal Muscle Leg	muscle
11	chr6:117458200-117460200	Weak transcription	Psoas Muscle	Psoas
12	chr6:117458400-117459600	Weak transcription	Colon Smooth Muscle	Colon
13	chr6:117459000-117459200	Enhancers	Fetal Heart	heart
14	chr6:117459000-117459600	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr6:117459000-117460400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr6:117459200-117460000	Weak transcription	Fetal Heart	heart
17	chr6:117459200-117463000	Weak transcription	Left Ventricle	heart
18	chr6:117459600-117460600	Enhancers	Stomach Smooth Muscle	stomach
19	chr6:117459600-117461200	Enhancers	Colon Smooth Muscle	Colon
20	chr6:117459600-117461400	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr6:117459800-117460000	Enhancers	Fetal Brain Male	brain
22	chr6:117459800-117460600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr6:117459800-117461000	Enhancers	HSMMtube	muscle
24	chr6:117460000-117461000	Enhancers	Rectal Smooth Muscle	rectum
25	chr6:117460000-117461400	Enhancers	Adipose Nuclei	Adipose
26	chr6:117460000-117461400	Enhancers	Fetal Heart	heart
27	chr6:117460200-117461000	Enhancers	Fetal Muscle Leg	muscle
28	chr6:117460200-117461000	Enhancers	Psoas Muscle	Psoas
29	chr6:117460200-117461200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr6:117460400-117461400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:117460600-117461000	Enhancers	Brain Hippocampus Middle	brain
32	chr6:117460800-117461200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr6:117461000-117462800	Weak transcription	Fetal Muscle Leg	muscle
34	chr6:117461000-117462800	Weak transcription	Psoas Muscle	Psoas
35	chr6:117461200-117467000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:117461400-117461800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr6:117461400-117462800	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr6:117461400-117463000	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr6:117461400-117463400	Weak transcription	Fetal Heart	heart
40	chr6:117462800-117463600	Enhancers	Psoas Muscle	Psoas
41	chr6:117462800-117463800	Enhancers	Fetal Muscle Leg	muscle
42	chr6:117462800-117464000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr6:117462800-117464800	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr6:117463000-117463400	Enhancers	H9 Cell Line	embryonic stem cell
45	chr6:117463000-117463600	Enhancers	Left Ventricle	heart
46	chr6:117463000-117463800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr6:117463000-117463800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr6:117463000-117464400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr6:117463000-117464800	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr6:117463200-117463400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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