Variant report

Variant	nsv1034168
Chromosome Location	chr6:167613263-167678902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1180)
CpG islands
(count:1648)
Chromatin interactive
region (count:13)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1180 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
12	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
13	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
16	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:167631950-167632087	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
21	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a
22	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:167626130-167626424	GM12878	blood:	n/a	n/a
24	BHLHE40	chr6:167637543-167637955	HepG2	liver:	n/a	n/a
25	BHLHE40	chr6:167629860-167630298	HepG2	liver:	n/a	n/a
26	BHLHE40	chr6:167617588-167617796	HepG2	liver:	n/a	n/a
27	BHLHE40	chr6:167617441-167617909	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:167617544-167617803	K562	blood:	n/a	n/a
29	BHLHE40	chr6:167631930-167632149	K562	blood:	n/a	n/a
30	BHLHE40	chr6:167626013-167626185	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:167617148-167617887	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:167631978-167632147	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:167631891-167632258	HepG2	liver:	n/a	n/a
34	BHLHE40	chr6:167629939-167630334	HepG2	liver:	n/a	n/a
35	BRCA1	chr6:167625284-167625312	HepG2	liver:	n/a	n/a
36	BRCA1	chr6:167624418-167624607	HepG2	liver:	n/a	n/a
37	BRCA1	chr6:167633650-167633694	HepG2	liver:	n/a	n/a
38	CBX3	chr6:167637348-167638006	HCT-116	colon:	n/a	n/a
39	CBX3	chr6:167669429-167669771	K562	blood:	n/a	n/a
40	CBX3	chr6:167617380-167617754	K562	blood:	n/a	n/a
41	CEBPB	chr6:167639685-167640004	H1-hESC	embryonic stem cell:	n/a	chr6:167639837-167639848 chr6:167639839-167639848 chr6:167639839-167639850
42	CEBPB	chr6:167624471-167624762	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:167629863-167630222	HepG2	liver:	n/a	n/a
44	CEBPB	chr6:167652443-167653271	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:167639673-167640002	HepG2	liver:	n/a	chr6:167639837-167639848 chr6:167639839-167639848 chr6:167639839-167639850
46	CEBPB	chr6:167629904-167630160	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:167629950-167630124	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:167665707-167665869	HepG2	liver:	n/a	chr6:167665793-167665804
49	CEBPB	chr6:167629456-167629648	HepG2	liver:	n/a	chr6:167629574-167629585 chr6:167629574-167629585 chr6:167629572-167629585
50	CEBPB	chr6:167639701-167639901	K562	blood:	n/a	chr6:167639837-167639848 chr6:167639839-167639848 chr6:167639839-167639850

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167649749-167649799	HRCEpiC	kidney:	n/a
2	chr6:167649749-167649799	HRCEpiC	kidney:	n/a
3	chr6:167617119-167617169	HPAEpiC	pulmonary alveolar:	n/a
4	chr6:167653982-167654032	AG04450	lung:	fetal
5	chr6:167649256-167649306	HMEC	breast:	n/a
6	chr6:167649384-167649434	T-47D	breast:	n/a
7	chr6:167655290-167655340	HUVEC	blood vessel:	n/a
8	chr6:167654977-167655027	Caco-2	colon:	n/a
9	chr6:167623149-167623199	A549	lung:	n/a
10	chr6:167649631-167649681	ECC-1	luminal epithelium:	n/a
11	chr6:167649539-167649589	SK-N-MC	brain:	n/a
12	chr6:167655290-167655340	GM19239	blood:	n/a
13	chr6:167649256-167649306	NHDF-neo	bronchial:	n/a
14	chr6:167616968-167617018	GM12878	blood:	n/a
15	chr6:167652028-167652078	NHBE	bronchial:	n/a
16	chr6:167652028-167652078	GM12892	blood:	n/a
17	chr6:167655290-167655340	HEK293	kidney:	embryo
18	chr6:167635072-167635122	U87	brain:	n/a
19	chr6:167632873-167632923	Jurkat	blood:	n/a
20	chr6:167617119-167617169	GM12878	blood:	n/a
21	chr6:167622441-167622491	SK-N-SH_RA	brain:	n/a
22	chr6:167652028-167652078	SK-N-SH	brain:	n/a
23	chr6:167623149-167623199	K562	blood:	n/a
24	chr6:167652028-167652078	HRE	kidney:	n/a
25	chr6:167649631-167649681	MCF10A-Er-Src	breast:	n/a
26	chr6:167649336-167649386	PrEC	prostate:	n/a
27	chr6:167649749-167649799	ECC-1	luminal epithelium:	n/a
28	chr6:167649539-167649589	IMR90	lung:	fetal
29	chr6:167633955-167634005	IMR90	lung:	fetal
30	chr6:167634139-167634189	AG04450	lung:	fetal
31	chr6:167649539-167649589	Caco-2	colon:	n/a
32	chr6:167655290-167655340	SKMC	muscle:	n/a
33	chr6:167622202-167622252	GM06990	blood:	n/a
34	chr6:167631788-167631838	SAEC	small airway:	n/a
35	chr6:167652028-167652078	GM06990	blood:	n/a
36	chr6:167633955-167634005	HIPEpiC	eye:	n/a
37	chr6:167649384-167649434	GM12892	blood:	n/a
38	chr6:167652028-167652078	AG04449	skin:	fetal
39	chr6:167655290-167655340	ovcar-3	ovarian:	n/a
40	chr6:167649384-167649434	GM12878	blood:	n/a
41	chr6:167649631-167649681	HEK293	kidney:	embryo
42	chr6:167649631-167649681	HCM	heart:	n/a
43	chr6:167634139-167634189	HEK293	kidney:	embryo
44	chr6:167632873-167632923	PFSK-1	brain:	n/a
45	chr6:167649539-167649589	MCF10A-Er-Src	breast:	n/a
46	chr6:167632873-167632923	HepG2	liver:	n/a
47	chr6:167661905-167661955	HRPEpiC	eye:	n/a
48	chr6:167653957-167654007	AG10803	skin:	n/a
49	chr6:167632873-167632923	BE2_C	brain:	n/a
50	chr6:167633955-167634005	NH-A	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
2	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
3	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:
4	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
5	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
6	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
7	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
8	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
9	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
10	chr6:167620399..167623068-chr6:167623897..167626646,2	K562	blood:
11	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
12	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
13	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921
2	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
3	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921
4	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921
5	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
6	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540

No data

Variant related genes	Relation type
ENSG00000228648	TF binding region
ENSG00000231720	TF binding region
ENSG00000216966	TF binding region
ENSG00000228648	CpG island
ENSG00000231720	CpG island
ENSG00000216966	CpG island
ENSG00000112494	chromatin interactions
ENSG00000216966	chromatin interactions
CYB5R4	miRNA target sites
CYBASC3	miRNA target sites

Extended variants
information (count: 3305 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3305 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9459912	chr6:167613263-167613264	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565485096	chr6:167613290-167613291	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532626401	chr6:167613309-167613310	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569683415	chr6:167613336-167613337	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35226021	chr6:167613351-167613352	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566077454	chr6:167613358-167613359	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536627304	chr6:167613365-167613366	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548340822	chr6:167613368-167613369	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567213913	chr6:167613410-167613411	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs56269544	chr6:167613412-167613413	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578139645	chr6:167613413-167613414	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537757609	chr6:167613422-167613423	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs555893100	chr6:167613424-167613425	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76769248	chr6:167613425-167613426	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6919991	chr6:167613452-167613453	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs6924592	chr6:167613455-167613456	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs553813247	chr6:167613479-167613480	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572071153	chr6:167613548-167613549	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181697422	chr6:167613550-167613551	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554279719	chr6:167613567-167613568	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185611793	chr6:167613645-167613646	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28459437	chr6:167613648-167613649	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs6920349	chr6:167613654-167613655	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs532737563	chr6:167613663-167613664	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541293416	chr6:167613677-167613678	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369850763	chr6:167613705-167613706	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs55893713	chr6:167613711-167613712	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs548523037	chr6:167613756-167613757	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113017369	chr6:167613758-167613759	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115665802	chr6:167613783-167613784	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549679465	chr6:167613785-167613786	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377521986	chr6:167613790-167613791	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538802674	chr6:167613833-167613834	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190022172	chr6:167613844-167613845	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149181565	chr6:167613863-167613864	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs62439202	chr6:167613929-167613930	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs140890273	chr6:167613935-167613936	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545552021	chr6:167613952-167613953	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576125631	chr6:167613953-167613954	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs397970122	chr6:167613959-167613960	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543478660	chr6:167613978-167613979	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs56092230	chr6:167614008-167614009	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs55997203	chr6:167614009-167614010	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182433453	chr6:167614025-167614026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs117677207	chr6:167614033-167614034	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541605130	chr6:167614054-167614055	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112588953	chr6:167614063-167614064	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144627906	chr6:167614071-167614072	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576326091	chr6:167614081-167614082	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541979291	chr6:167614085-167614086	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167610600-167615400	Weak transcription	Fetal Brain Male	brain
2	chr6:167612800-167615000	Strong transcription	Fetal Intestine Small	intestine
3	chr6:167613000-167613600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:167613000-167613800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:167613000-167616600	Enhancers	Placenta Amnion	Placenta Amnion
6	chr6:167613600-167613800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:167613800-167614400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:167613800-167622200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:167614000-167615400	Enhancers	HepG2	liver
10	chr6:167614200-167614400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr6:167614400-167614800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:167614400-167623200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:167614800-167616400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:167615000-167616800	Weak transcription	Fetal Intestine Small	intestine
15	chr6:167615400-167616400	Weak transcription	HepG2	liver
16	chr6:167615400-167617400	Enhancers	Fetal Brain Male	brain
17	chr6:167615800-167616200	Enhancers	Fetal Lung	lung
18	chr6:167615800-167628800	Weak transcription	Right Atrium	heart
19	chr6:167616400-167617000	Enhancers	HepG2	liver
20	chr6:167616400-167617400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:167616400-167617600	Enhancers	Rectal Smooth Muscle	rectum
22	chr6:167616600-167617200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr6:167616600-167617800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr6:167616600-167618400	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr6:167616800-167617200	Enhancers	Stomach Smooth Muscle	stomach
26	chr6:167616800-167617400	Bivalent Enhancer	K562	blood
27	chr6:167616800-167617600	Enhancers	Fetal Intestine Small	intestine
28	chr6:167617000-167617400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr6:167617000-167617400	Enhancers	Liver	Liver
30	chr6:167617000-167617400	Enhancers	Fetal Heart	heart
31	chr6:167617000-167617400	Enhancers	Fetal Intestine Large	intestine
32	chr6:167617000-167617400	Enhancers	Lung	lung
33	chr6:167617000-167617400	Active TSS	A549	lung
34	chr6:167617000-167617400	Flanking Active TSS	HepG2	liver
35	chr6:167617000-167617400	Enhancers	NH-A	brain
36	chr6:167617200-167617400	Enhancers	Colon Smooth Muscle	Colon
37	chr6:167617200-167617400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
38	chr6:167617400-167618200	Weak transcription	NH-A	brain
39	chr6:167617400-167618600	Weak transcription	Fetal Brain Male	brain
40	chr6:167617400-167619000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr6:167617400-167620800	Enhancers	HepG2	liver
42	chr6:167617400-167622400	Weak transcription	Fetal Intestine Large	intestine
43	chr6:167617600-167618000	Weak transcription	Fetal Intestine Small	intestine
44	chr6:167617600-167618000	Weak transcription	Rectal Smooth Muscle	rectum
45	chr6:167617600-167618200	Weak transcription	Colon Smooth Muscle	Colon
46	chr6:167618000-167619000	Enhancers	Fetal Intestine Small	intestine
47	chr6:167618000-167619000	Enhancers	Rectal Smooth Muscle	rectum
48	chr6:167618200-167618400	Enhancers	Colon Smooth Muscle	Colon
49	chr6:167618400-167618600	Enhancers	NH-A	brain
50	chr6:167618400-167619000	Enhancers	Placenta Amnion	Placenta Amnion

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