Variant report

Variant	nsv481692
Chromosome Location	chr6:163134854-163155124
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	chr6:163148619-163149118	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:163148702-163148902	K562	blood:	n/a	n/a
3	ATF1	chr6:163148753-163149159	K562	blood:	n/a	n/a
4	ATF2	chr6:163148711-163149191	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
5	ATF2	chr6:163148704-163149149	GM12878	blood:	n/a	chr6:163148957-163148968
6	ATF2	chr6:163148726-163149178	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
7	ATF2	chr6:163148705-163149166	GM12878	blood:	n/a	chr6:163148957-163148968
8	ATF3	chr6:163148710-163149085	K562	blood:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
9	ATF3	chr6:163148729-163149180	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
10	ATF3	chr6:163148738-163149179	K562	blood:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
11	ATF3	chr6:163148498-163149119	HepG2	liver:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
12	ATF3	chr6:163148789-163149068	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
13	BACH1	chr6:163148603-163148838	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:163149073-163149266	K562	blood:	n/a	n/a
15	BCLAF1	chr6:163148707-163149054	GM12878	blood:	n/a	chr6:163148747-163148760
16	BHLHE40	chr6:163148582-163149115	K562	blood:	n/a	chr6:163148747-163148763
17	BHLHE40	chr6:163148554-163149138	HepG2	liver:	n/a	chr6:163148747-163148763
18	BHLHE40	chr6:163148697-163149088	GM12878	blood:	n/a	chr6:163148747-163148763
19	BRCA1	chr6:163148845-163149085	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr6:163148841-163149053	HepG2	liver:	n/a	n/a
21	CBX3	chr6:163148516-163149230	K562	blood:	n/a	n/a
22	CCNT2	chr6:163148390-163149101	K562	blood:	n/a	chr6:163148913-163148922 chr6:163148970-163148979 chr6:163149075-163149084
23	CEBPB	chr6:163148686-163149168	A549	lung:	n/a	n/a
24	CEBPB	chr6:163148750-163149181	K562	blood:	n/a	n/a
25	CEBPB	chr6:163148563-163149157	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:163148771-163149153	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:163146789-163146918	HepG2	liver:	n/a	chr6:163146839-163146850 chr6:163146838-163146849 chr6:163146838-163146849
28	CEBPB	chr6:163148788-163149168	A549	lung:	n/a	n/a
29	CEBPB	chr6:163148734-163149200	MCF-7	breast:	n/a	n/a
30	CEBPB	chr6:163148779-163149062	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:163148713-163149149	IMR90	lung:	n/a	n/a
32	CEBPB	chr6:163148800-163149065	K562	blood:	n/a	n/a
33	CEBPB	chr6:163148769-163149119	MCF-7	breast:	n/a	n/a
34	CEBPB	chr6:163148643-163149149	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr6:163148769-163149149	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr6:163148738-163149145	K562	blood:	n/a	n/a
37	CEBPD	chr6:163148838-163149102	HepG2	liver:	n/a	n/a
38	CEBPD	chr6:163148521-163149131	HepG2	liver:	n/a	n/a
39	CHD1	chr6:163148818-163148888	GM12878	blood:	n/a	n/a
40	CHD2	chr6:163148677-163149145	HepG2	liver:	n/a	chr6:163149073-163149083
41	CHD2	chr6:163148700-163149167	H1-hESC	embryonic stem cell:	n/a	chr6:163149073-163149083
42	CHD2	chr6:163148657-163149132	K562	blood:	n/a	chr6:163149073-163149083
43	CHD2	chr6:163148669-163149124	GM12878	blood:	n/a	chr6:163149073-163149083
44	CHD2	chr6:163148643-163149138	Hela-S3	cervix:	n/a	chr6:163149073-163149083
45	CREB1	chr6:163148576-163149222	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr6:163148616-163149342	K562	blood:	n/a	n/a
47	CREB1	chr6:163148720-163149209	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr6:163148680-163149184	GM12878	blood:	n/a	n/a
49	CREB1	chr6:163148581-163149237	HepG2	liver:	n/a	n/a
50	CREB1	chr6:163148419-163149170	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163147737-163147787	HCT-116	colon:	n/a
2	chr6:163147737-163147787	HL-60	blood:	n/a
3	chr6:163147737-163147787	BE2_C	brain:	n/a
4	chr6:163148777-163148827	Hepatocyte	liver:	n/a
5	chr6:163148777-163148827	NB4	blood:	n/a
6	chr6:163149169-163149219	LNCaP	prostate:	n/a
7	chr6:163147737-163147787	HCT-116	colon:	n/a
8	chr6:163147737-163147787	HL-60	blood:	n/a
9	chr6:163147737-163147787	BE2_C	brain:	n/a
10	chr6:163148777-163148827	Hepatocyte	liver:	n/a
11	chr6:163148777-163148827	NB4	blood:	n/a
12	chr6:163149169-163149219	LNCaP	prostate:	n/a
13	chr6:163149674-163149724	SK-N-MC	brain:	n/a
14	chr6:163149674-163149724	AG09309	skin:	n/a
15	chr6:163149167-163149217	CMK	blood:	n/a
16	chr6:163148290-163148340	NHDF-neo	bronchial:	n/a
17	chr6:163149320-163149370	SAEC	small airway:	n/a
18	chr6:163148718-163148768	NHDF-neo	bronchial:	n/a
19	chr6:163148903-163148953	HRE	kidney:	n/a
20	chr6:163146217-163146267	HCT-116	colon:	n/a
21	chr6:163148501-163148551	HCPEpiC	choroid plexus:	n/a
22	chr6:163147733-163147783	U87	brain:	n/a
23	chr6:163148718-163148768	HCT-116	colon:	n/a
24	chr6:163149167-163149217	GM12891	blood:	n/a
25	chr6:163148290-163148340	GM12878	blood:	n/a
26	chr6:163149169-163149219	NHDF-neo	bronchial:	n/a
27	chr6:163149320-163149370	HCT-116	colon:	n/a
28	chr6:163148501-163148551	T-47D	breast:	n/a
29	chr6:163149674-163149724	T-47D	breast:	n/a
30	chr6:163146217-163146267	RPTEC	kidney:	n/a
31	chr6:163149169-163149219	PrEC	prostate:	n/a
32	chr6:163148777-163148827	HUVEC	blood vessel:	n/a
33	chr6:163148022-163148072	SK-N-SH	brain:	n/a
34	chr6:163148018-163148068	K562	blood:	n/a
35	chr6:163149320-163149370	HIPEpiC	eye:	n/a
36	chr6:163148903-163148953	GM06990	blood:	n/a
37	chr6:163149320-163149370	BE2_C	brain:	n/a
38	chr6:163148022-163148072	HCM	heart:	n/a
39	chr6:163149453-163149503	U87	brain:	n/a
40	chr6:163146217-163146267	NB4	blood:	n/a
41	chr6:163148501-163148551	AG09319	gingival:	n/a
42	chr6:163147999-163148049	GM19239	blood:	n/a
43	chr6:163146217-163146267	GM12892	blood:	n/a
44	chr6:163149320-163149370	SK-N-MC	brain:	n/a
45	chr6:163148290-163148340	SK-N-SH	brain:	n/a
46	chr6:163149320-163149370	AG04450	lung:	fetal
47	chr6:163148290-163148340	AG04450	lung:	fetal
48	chr6:163147999-163148049	HCF	heart:	n/a
49	chr6:163148018-163148068	IMR90	lung:	fetal
50	chr6:163149320-163149370	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163138657..163141393-chr6:163146602..163148183,2	MCF-7	breast:
2	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
3	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
4	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
5	chr6:163139294..163141851-chr6:163147296..163150092,3	MCF-7	breast:
6	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
7	chr6:163138973..163143825-chr6:163144102..163148168,6	K562	blood:
8	chr6:163136674..163141943-chr6:163143603..163148822,6	K562	blood:
9	chr6:163142325..163145868-chr6:163146633..163149200,3	K562	blood:

Variant related genes	Relation type
PACRG	TF binding region
PARK2	TF binding region
PACRG	CpG island
PARK2	CpG island
ENSG00000112530	chromatin interactions
ENSG00000185345	chromatin interactions

Extended variants
information (count: 819 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:819 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530266127	chr6:163134923-163134924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs2803057	chr6:163134931-163134932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566868180	chr6:163135064-163135065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532662830	chr6:163135073-163135074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552859387	chr6:163135076-163135077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192790076	chr6:163135083-163135084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538035507	chr6:163135167-163135168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554787027	chr6:163135168-163135169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567768266	chr6:163135178-163135179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533648344	chr6:163135196-163135197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553453230	chr6:163135200-163135201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576793403	chr6:163135223-163135224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11967632	chr6:163135225-163135226	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs2849515	chr6:163135233-163135234	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs542044123	chr6:163135256-163135257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184928968	chr6:163135273-163135274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2849514	chr6:163135289-163135290	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs534731480	chr6:163135321-163135322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540746848	chr6:163135366-163135367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560262669	chr6:163135386-163135387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532519104	chr6:163135387-163135388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552326341	chr6:163135423-163135424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376246300	chr6:163135443-163135444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371404284	chr6:163135459-163135460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555860361	chr6:163135460-163135461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568464019	chr6:163135478-163135479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140595052	chr6:163135486-163135487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568328657	chr6:163135548-163135549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533614526	chr6:163135594-163135595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150421968	chr6:163135596-163135597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145574192	chr6:163135615-163135616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7748649	chr6:163135635-163135636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9346928	chr6:163135652-163135653	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs7752539	chr6:163135757-163135758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2849513	chr6:163135797-163135798	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs555567334	chr6:163135814-163135815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370971456	chr6:163135851-163135852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs116103214	chr6:163135872-163135873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540898916	chr6:163136020-163136021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149539678	chr6:163136031-163136032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560622635	chr6:163136043-163136044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577310707	chr6:163136057-163136058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189451010	chr6:163136116-163136117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562746358	chr6:163136129-163136130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531848860	chr6:163136139-163136140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548491958	chr6:163136166-163136167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562071757	chr6:163136170-163136171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557266473	chr6:163136222-163136223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181642099	chr6:163136223-163136224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575539448	chr6:163136287-163136288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:544 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163119800-163138000	Weak transcription	Aorta	Aorta
2	chr6:163127800-163136800	Weak transcription	Ovary	ovary
3	chr6:163128000-163137800	Weak transcription	Fetal Brain Male	brain
4	chr6:163132800-163142400	Weak transcription	Psoas Muscle	Psoas
5	chr6:163133000-163138000	Weak transcription	Left Ventricle	heart
6	chr6:163133000-163142200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr6:163133600-163138000	Weak transcription	Pancreas	Pancrea
8	chr6:163134800-163136400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr6:163135000-163135800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:163135000-163135800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr6:163135000-163136000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:163135000-163136200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr6:163135000-163136400	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr6:163135000-163137000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr6:163135200-163135600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:163135200-163135800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr6:163135400-163136400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr6:163135600-163148200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:163135800-163140200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr6:163136400-163140400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr6:163136400-163140600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr6:163136800-163137000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:163136800-163137000	Enhancers	Ovary	ovary
24	chr6:163137000-163148000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr6:163137800-163138000	Enhancers	Fetal Brain Male	brain
26	chr6:163138000-163138200	ZNF genes & repeats	Pancreas	Pancrea
27	chr6:163138000-163138400	ZNF genes & repeats	Aorta	Aorta
28	chr6:163138000-163138400	ZNF genes & repeats	Left Ventricle	heart
29	chr6:163138200-163138400	ZNF genes & repeats	Fetal Intestine Small	intestine
30	chr6:163138200-163145800	Weak transcription	Pancreas	Pancrea
31	chr6:163138400-163146000	Weak transcription	Left Ventricle	heart
32	chr6:163138400-163148000	Weak transcription	Aorta	Aorta
33	chr6:163138600-163139000	Weak transcription	Fetal Intestine Small	intestine
34	chr6:163139800-163140800	Enhancers	Fetal Muscle Leg	muscle
35	chr6:163140200-163140600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr6:163140200-163140600	Enhancers	Fetal Heart	heart
37	chr6:163140200-163140800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr6:163140200-163140800	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr6:163140200-163140800	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr6:163140400-163140600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr6:163140400-163140800	Enhancers	HSMMtube	muscle
42	chr6:163140600-163140800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr6:163140600-163141800	Weak transcription	Fetal Heart	heart
44	chr6:163140600-163144400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr6:163140800-163142400	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr6:163140800-163144200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr6:163140800-163144200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr6:163140800-163144800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr6:163140800-163147600	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr6:163141800-163142400	Enhancers	Fetal Heart	heart

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