Variant report

Variant	esv2757190
Chromosome Location	chr6:117464048-117609529
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:912)
CpG islands
(count:1648)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:912 , 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	chr6:117593759-117594104	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	chr6:117592194-117592308	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:117591194-117591325	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:117561663-117561856	GM12878	blood:	n/a	n/a
8	CBX3	chr6:117488717-117489231	HCT-116	colon:	n/a	n/a
9	CCNT2	chr6:117476295-117476440	K562	blood:	n/a	n/a
10	CCNT2	chr6:117538241-117538436	K562	blood:	n/a	n/a
11	CEBPB	chr6:117591356-117591416	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr6:117560505-117560830	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:117601351-117601551	HepG2	liver:	n/a	chr6:117601467-117601478
14	CEBPB	chr6:117516940-117517351	HCT-116	colon:	n/a	chr6:117517085-117517096
15	CEBPB	chr6:117549961-117550163	HepG2	liver:	n/a	chr6:117550075-117550086
16	CEBPB	chr6:117516918-117517266	Hela-S3	cervix:	n/a	chr6:117517085-117517096
17	CEBPB	chr6:117587004-117587185	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr6:117516814-117517281	HCT-116	colon:	n/a	chr6:117517085-117517096
19	CEBPB	chr6:117554591-117554700	A549	lung:	n/a	chr6:117554655-117554666
20	CEBPB	chr6:117516923-117517217	HepG2	liver:	n/a	chr6:117517085-117517096
21	CEBPB	chr6:117486492-117486632	HepG2	liver:	n/a	chr6:117486549-117486560 chr6:117486549-117486562 chr6:117486551-117486562
22	CEBPB	chr6:117554489-117554800	HepG2	liver:	n/a	chr6:117554655-117554666
23	CEBPB	chr6:117548007-117548706	HepG2	liver:	n/a	chr6:117548497-117548508 chr6:117548495-117548506
24	CEBPB	chr6:117516938-117517254	H1-hESC	embryonic stem cell:	n/a	chr6:117517085-117517096
25	CEBPB	chr6:117550047-117550129	A549	lung:	n/a	chr6:117550075-117550086
26	CHD1	chr6:117591181-117591739	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr6:117592127-117592222	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr6:117586262-117586360	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr6:117591297-117591320	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr6:117603480-117603676	K562	blood:	n/a	n/a
31	CREB1	chr6:117586600-117587155	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr6:117585407-117586358	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTBP2	chr6:117586727-117587425	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTBP2	chr6:117591168-117592322	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr6:117602173-117602358	LNCaP	prostate:	n/a	n/a
36	CTCF	chr6:117602180-117602330	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr6:117510000-117510150	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:117602205-117602359	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:117602200-117602350	HRE	kidney:	n/a	n/a
40	CTCF	chr6:117589454-117589561	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:117509969-117510282	MCF-7	breast:	n/a	chr6:117510166-117510184
42	CTCF	chr6:117589400-117589550	GM06990	blood:	n/a	n/a
43	CTCF	chr6:117586680-117586830	HMEC	breast:	n/a	chr6:117586701-117586714
44	CTCF	chr6:117510080-117510230	AG10803	skin:	n/a	chr6:117510166-117510184
45	CTCF	chr6:117488843-117488917	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:117510120-117510270	HCFaa	heart:	n/a	chr6:117510166-117510184
47	CTCF	chr6:117602200-117602350	HCT-116	colon:	n/a	n/a
48	CTCF	chr6:117510040-117510190	BJ	skin:	n/a	chr6:117510166-117510184
49	CTCF	chr6:117586380-117586530	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr6:117489020-117489170	HMEC	breast:	n/a	chr6:117489048-117489056

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:117583893-117583943	ProgFib	skin:	n/a
2	chr6:117583893-117583943	ProgFib	skin:	n/a
3	chr6:117594700-117594750	AG04449	skin:	fetal
4	chr6:117591534-117591584	GM12878	blood:	n/a
5	chr6:117589651-117589701	SKMC	muscle:	n/a
6	chr6:117586918-117586968	BE2_C	brain:	n/a
7	chr6:117586225-117586275	BJ	skin:	n/a
8	chr6:117584665-117584715	AG09309	skin:	n/a
9	chr6:117587588-117587638	HEEpiC	esophagus:	n/a
10	chr6:117583893-117583943	AG04449	skin:	fetal
11	chr6:117589651-117589701	CMK	blood:	n/a
12	chr6:117586538-117586588	SK-N-SH	brain:	n/a
13	chr6:117589651-117589701	HRPEpiC	eye:	n/a
14	chr6:117587155-117587205	PrEC	prostate:	n/a
15	chr6:117583181-117583231	RPTEC	kidney:	n/a
16	chr6:117586575-117586625	HRCEpiC	kidney:	n/a
17	chr6:117591684-117591734	HRE	kidney:	n/a
18	chr6:117583893-117583943	Caco-2	colon:	n/a
19	chr6:117589651-117589701	RPTEC	kidney:	n/a
20	chr6:117585815-117585865	ovcar-3	ovarian:	n/a
21	chr6:117584596-117584646	CMK	blood:	n/a
22	chr6:117587588-117587638	HRE	kidney:	n/a
23	chr6:117584665-117584715	GM12878	blood:	n/a
24	chr6:117586681-117586731	T-47D	breast:	n/a
25	chr6:117584596-117584646	HIPEpiC	eye:	n/a
26	chr6:117594700-117594750	BE2_C	brain:	n/a
27	chr6:117586666-117586716	NHBE	bronchial:	n/a
28	chr6:117585479-117585529	HCT-116	colon:	n/a
29	chr6:117584715-117584765	PFSK-1	brain:	n/a
30	chr6:117589651-117589701	HL-60	blood:	n/a
31	chr6:117592262-117592312	Caco-2	colon:	n/a
32	chr6:117591534-117591584	SK-N-SH_RA	brain:	n/a
33	chr6:117585479-117585529	HRCEpiC	kidney:	n/a
34	chr6:117583893-117583943	GM12892	blood:	n/a
35	chr6:117586817-117586867	GM19239	blood:	n/a
36	chr6:117591433-117591483	LNCaP	prostate:	n/a
37	chr6:117586817-117586867	NHDF-neo	bronchial:	n/a
38	chr6:117584815-117584865	A549	lung:	n/a
39	chr6:117583893-117583943	HRPEpiC	eye:	n/a
40	chr6:117591534-117591584	AG04449	skin:	fetal
41	chr6:117591684-117591734	GM06990	blood:	n/a
42	chr6:117583893-117583943	K562	blood:	n/a
43	chr6:117589651-117589701	IMR90	lung:	fetal
44	chr6:117584715-117584765	HAEpiC	amniotic membrane:	n/a
45	chr6:117592358-117592408	GM12892	blood:	n/a
46	chr6:117586538-117586588	NB4	blood:	n/a
47	chr6:117586225-117586275	NHBE	bronchial:	n/a
48	chr6:117592358-117592408	AoSMC	blood vessel:	n/a
49	chr6:117586918-117586968	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:117586225-117586275	SK-N-SH_RA	brain:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:117601835..117602502-chr6:117638433..117639008,2	MCF-7	breast:
2	chr6:117293198..117294084-chr6:117602223..117602832,3	MCF-7	breast:
3	chr6:116710278..116712360-chr6:117478553..117480106,2	K562	blood:
4	chr6:117292562..117293807-chr6:117509373..117510214,3	MCF-7	breast:
5	chr6:117290291..117290928-chr6:117516415..117517089,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ROS1-2	chr6:117585738-117585864	NONHSAT114666
2	lnc-ROS1-2	chr6:117583516-117584346	NONHSAT114666

No data

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

Extended variants
information (count: 4175 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:4175 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17078856	chr6:117464048-117464049	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146293937	chr6:117464132-117464133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12215962	chr6:117464133-117464134	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs534017109	chr6:117464171-117464172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1405211	chr6:117464172-117464173	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs573750918	chr6:117464181-117464182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138487484	chr6:117464206-117464207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs475755	chr6:117464208-117464209	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs577241936	chr6:117464222-117464223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146146498	chr6:117464241-117464242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187244985	chr6:117464284-117464285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527425521	chr6:117464286-117464287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542357992	chr6:117464318-117464319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562313579	chr6:117464367-117464368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529427886	chr6:117464408-117464409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573999444	chr6:117464436-117464437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34640664	chr6:117464477-117464478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569540860	chr6:117464490-117464491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs9481691	chr6:117464494-117464495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555640581	chr6:117464550-117464551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533643692	chr6:117464566-117464567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114866091	chr6:117464576-117464577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs55975555	chr6:117464614-117464615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs55999473	chr6:117464616-117464617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566862834	chr6:117464678-117464679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564335317	chr6:117464737-117464738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192913666	chr6:117464778-117464779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567462204	chr6:117464836-117464837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537617772	chr6:117464842-117464843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555919715	chr6:117464855-117464856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577550644	chr6:117464867-117464868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185682819	chr6:117464874-117464875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553401207	chr6:117464892-117464893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571903265	chr6:117464929-117464930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369397536	chr6:117464930-117464931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542717944	chr6:117464976-117464977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560788468	chr6:117464993-117464994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62430543	chr6:117465018-117465019	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs373125381	chr6:117465026-117465027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563055361	chr6:117465046-117465047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190541810	chr6:117465061-117465062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552099251	chr6:117465078-117465079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560491112	chr6:117465101-117465102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527645549	chr6:117465110-117465111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180824105	chr6:117465111-117465112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74649926	chr6:117465113-117465114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556234569	chr6:117465122-117465123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538323466	chr6:117465128-117465129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139930251	chr6:117465190-117465191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376315598	chr6:117465318-117465319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1007 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117461200-117467000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:117462800-117464800	Enhancers	Skeletal Muscle Female	skeletal muscle
3	chr6:117463000-117464400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr6:117463000-117464800	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr6:117463400-117464600	Enhancers	Fetal Heart	heart
6	chr6:117463600-117464600	Weak transcription	Left Ventricle	heart
7	chr6:117463800-117464400	Weak transcription	Fetal Muscle Leg	muscle
8	chr6:117464000-117464600	Enhancers	Psoas Muscle	Psoas
9	chr6:117464400-117464600	Enhancers	Fetal Muscle Leg	muscle
10	chr6:117464400-117464800	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr6:117464600-117464800	Enhancers	Left Ventricle	heart
12	chr6:117464600-117478000	Weak transcription	Psoas Muscle	Psoas
13	chr6:117466200-117467200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr6:117477200-117479000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:117477600-117478200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:117477600-117478200	Enhancers	HSMMtube	muscle
17	chr6:117477600-117478400	Enhancers	Right Ventricle	heart
18	chr6:117477600-117479000	Enhancers	Fetal Muscle Leg	muscle
19	chr6:117477600-117479000	Enhancers	Fetal Stomach	stomach
20	chr6:117477600-117479000	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr6:117477600-117479200	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr6:117477800-117479000	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr6:117477800-117479200	Enhancers	HSMM	muscle
24	chr6:117478000-117478200	Enhancers	Left Ventricle	heart
25	chr6:117478000-117478200	Enhancers	Psoas Muscle	Psoas
26	chr6:117478000-117479000	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr6:117478200-117478400	Flanking Active TSS	HSMMtube	muscle
28	chr6:117478200-117478600	Weak transcription	Psoas Muscle	Psoas
29	chr6:117478200-117479000	Enhancers	Fetal Heart	heart
30	chr6:117478200-117479000	Enhancers	Stomach Smooth Muscle	stomach
31	chr6:117478400-117478800	Active TSS	HSMMtube	muscle
32	chr6:117478600-117479000	Enhancers	Psoas Muscle	Psoas
33	chr6:117478800-117479000	Enhancers	Gastric	stomach
34	chr6:117478800-117479000	Enhancers	Left Ventricle	heart
35	chr6:117478800-117479000	Flanking Active TSS	HSMMtube	muscle
36	chr6:117479000-117479400	Enhancers	HSMMtube	muscle
37	chr6:117479000-117486400	Weak transcription	Fetal Muscle Leg	muscle
38	chr6:117479000-117487200	Weak transcription	Fetal Stomach	stomach
39	chr6:117486000-117486200	Enhancers	HSMMtube	muscle
40	chr6:117486200-117487000	Weak transcription	HSMMtube	muscle
41	chr6:117486400-117491200	Enhancers	Fetal Muscle Leg	muscle
42	chr6:117487000-117487800	Enhancers	HSMMtube	muscle
43	chr6:117487200-117487400	Enhancers	Fetal Stomach	stomach
44	chr6:117487200-117487400	Weak transcription	Right Atrium	heart
45	chr6:117487200-117489600	Enhancers	HSMM	muscle
46	chr6:117487200-117491200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr6:117487400-117487600	Enhancers	Esophagus	oesophagus
48	chr6:117487400-117487600	Enhancers	Left Ventricle	heart
49	chr6:117487400-117487600	Enhancers	Right Atrium	heart
50	chr6:117487400-117488000	Weak transcription	Fetal Stomach	stomach

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