Variant report

Variant	nsv1030651
Chromosome Location	chr6:64028392-64102045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:825)
CpG islands
(count:183)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:825 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:64061842-64062271	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:64058006-64058016	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:64062913-64063349	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:64101330-64101949	HepG2	liver:	n/a	n/a
5	ATF1	chr6:64083127-64083308	K562	blood:	n/a	n/a
6	ATF2	chr6:64057519-64057901	GM12878	blood:	n/a	n/a
7	ATF2	chr6:64062307-64063405	GM12878	blood:	n/a	n/a
8	ATF2	chr6:64061990-64063362	GM12878	blood:	n/a	n/a
9	ATF3	chr6:64062702-64063222	GM12878	blood:	n/a	n/a
10	BATF	chr6:64062394-64062984	GM12878	blood:	n/a	n/a
11	BATF	chr6:64057524-64057796	GM12878	blood:	n/a	n/a
12	BATF	chr6:64086526-64086830	GM12878	blood:	n/a	chr6:64086675-64086686
13	BATF	chr6:64057503-64057905	GM12878	blood:	n/a	n/a
14	BCL11A	chr6:64093726-64094062	GM12878	blood:	n/a	chr6:64093917-64093926
15	BCL11A	chr6:64062412-64062975	GM12878	blood:	n/a	n/a
16	BCL11A	chr6:64062308-64063061	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:64062312-64063311	GM12878	blood:	n/a	n/a
18	BCLAF1	chr6:64062213-64063430	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:64101403-64101854	HepG2	liver:	n/a	n/a
20	BHLHE40	chr6:64061987-64063282	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:64093740-64094165	GM12878	blood:	n/a	n/a
22	BRCA1	chr6:64061717-64062393	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr6:64057431-64057955	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr6:64057343-64058015	HCT-116	colon:	n/a	chr6:64057602-64057613
25	CCNT2	chr6:64101527-64101618	K562	blood:	n/a	n/a
26	CEBPB	chr6:64061923-64062415	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr6:64062632-64063362	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr6:64065384-64065879	A549	lung:	n/a	chr6:64065639-64065650
29	CEBPB	chr6:64101389-64101791	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:64098031-64098201	A549	lung:	n/a	chr6:64098116-64098125 chr6:64098116-64098125
31	CEBPB	chr6:64072861-64072981	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:64065562-64065813	HepG2	liver:	n/a	chr6:64065639-64065650
33	CEBPB	chr6:64065399-64065779	MCF-7	breast:	n/a	chr6:64065639-64065650
34	CEBPB	chr6:64098075-64098264	HepG2	liver:	n/a	chr6:64098116-64098125 chr6:64098116-64098125
35	CEBPB	chr6:64065498-64065825	A549	lung:	n/a	chr6:64065639-64065650
36	CEBPB	chr6:64062286-64063500	GM12878	blood:	n/a	n/a
37	CEBPB	chr6:64062990-64063317	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:64057333-64058060	HCT-116	colon:	n/a	chr6:64057610-64057622
39	CEBPB	chr6:64062474-64063043	GM12878	blood:	n/a	n/a
40	CEBPB	chr6:64057464-64057979	A549	lung:	n/a	chr6:64057610-64057622
41	CEBPB	chr6:64101370-64101827	HepG2	liver:	n/a	n/a
42	CEBPB	chr6:64065512-64065808	A549	lung:	n/a	chr6:64065639-64065650
43	CEBPB	chr6:64065537-64065723	HepG2	liver:	n/a	chr6:64065639-64065650
44	CEBPB	chr6:64065437-64065832	Hela-S3	cervix:	n/a	chr6:64065639-64065650
45	CHD2	chr6:64093731-64094180	GM12878	blood:	n/a	n/a
46	CHD2	chr6:64065435-64065635	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr6:64062460-64063288	GM12878	blood:	n/a	n/a
48	CTCF	chr6:64063060-64063210	GM12864	blood:	n/a	chr6:64063110-64063128 chr6:64063112-64063133
49	CTCF	chr6:64063020-64063170	NHEK	skin:	n/a	chr6:64063110-64063128 chr6:64063112-64063133
50	CTCF	chr6:64062992-64063237	Hela-S3	cervix:	n/a	chr6:64063110-64063128 chr6:64063112-64063133

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:64029870-64029920	AG10803	skin:	n/a
2	chr6:64029870-64029920	PrEC	prostate:	n/a
3	chr6:64042706-64042756	HEEpiC	esophagus:	n/a
4	chr6:64030429-64030479	BE2_C	brain:	n/a
5	chr6:64042706-64042756	HCT-116	colon:	n/a
6	chr6:64030429-64030479	RPTEC	kidney:	n/a
7	chr6:64030429-64030479	BJ	skin:	n/a
8	chr6:64030429-64030479	SK-N-SH_RA	brain:	n/a
9	chr6:64042706-64042756	SK-N-SH	brain:	n/a
10	chr6:64042706-64042756	HMEC	breast:	n/a
11	chr6:64029870-64029920	HCPEpiC	choroid plexus:	n/a
12	chr6:64042706-64042756	Caco-2	colon:	n/a
13	chr6:64042706-64042756	PrEC	prostate:	n/a
14	chr6:64029870-64029920	HEEpiC	esophagus:	n/a
15	chr6:64029870-64029920	Jurkat	blood:	n/a
16	chr6:64029870-64029920	ovcar-3	ovarian:	n/a
17	chr6:64042706-64042756	ovcar-3	ovarian:	n/a
18	chr6:64030429-64030479	HCPEpiC	choroid plexus:	n/a
19	chr6:64030429-64030479	ProgFib	skin:	n/a
20	chr6:64029870-64029920	AoSMC	blood vessel:	n/a
21	chr6:64042706-64042756	MCF10A-Er-Src	breast:	n/a
22	chr6:64042706-64042756	HRE	kidney:	n/a
23	chr6:64029870-64029920	HCF	heart:	n/a
24	chr6:64042706-64042756	HNPCEpiC	eye:	n/a
25	chr6:64029870-64029920	HPAEpiC	pulmonary alveolar:	n/a
26	chr6:64030429-64030479	SKMC	muscle:	n/a
27	chr6:64029870-64029920	PANC-1	pancreas:	n/a
28	chr6:64030429-64030479	GM19239	blood:	n/a
29	chr6:64042706-64042756	NB4	blood:	n/a
30	chr6:64030429-64030479	HAEpiC	amniotic membrane:	n/a
31	chr6:64030429-64030479	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:64029870-64029920	SKMC	muscle:	n/a
33	chr6:64042706-64042756	SAEC	small airway:	n/a
34	chr6:64042706-64042756	ECC-1	luminal epithelium:	n/a
35	chr6:64030429-64030479	GM12891	blood:	n/a
36	chr6:64042706-64042756	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:64042706-64042756	SKMC	muscle:	n/a
38	chr6:64029870-64029920	LNCaP	prostate:	n/a
39	chr6:64030429-64030479	LNCaP	prostate:	n/a
40	chr6:64029870-64029920	AG04449	skin:	fetal
41	chr6:64029870-64029920	NT2-D1	testis:	n/a
42	chr6:64042706-64042756	NT2-D1	testis:	n/a
43	chr6:64042706-64042756	AG09309	skin:	n/a
44	chr6:64042706-64042756	MCF-7	breast:	n/a
45	chr6:64029870-64029920	IMR90	lung:	fetal
46	chr6:64030429-64030479	HL-60	blood:	n/a
47	chr6:64029870-64029920	MCF-7	breast:	n/a
48	chr6:64030429-64030479	PANC-1	pancreas:	n/a
49	chr6:64042706-64042756	LNCaP	prostate:	n/a
50	chr6:64029870-64029920	HepG2	liver:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:64060326..64062411-chr6:64092797..64095365,2	K562	blood:
2	chr6:64060326..64062411-chr6:64092797..64095365,2	K562	blood:
3	chr6:64062639..64063365-chr6:64283555..64284772,4	MCF-7	breast:
4	chr6:64028950..64031387-chr6:64282272..64283955,2	MCF-7	breast:
5	chr6:64052335..64054049-chr6:64060592..64063155,2	MCF-7	breast:
6	chr6:64082531..64084931-chr6:64282447..64284673,2	MCF-7	breast:
7	chr6:64062103..64065068-chr6:64510364..64512443,2	MCF-7	breast:
8	chr6:64061851..64067000-chr6:64282014..64286349,7	MCF-7	breast:
9	chr6:64062641..64063566-chr6:64308201..64309203,4	MCF-7	breast:
10	chr6:64059286..64067591-chr6:64279675..64285580,14	MCF-7	breast:
11	chr6:64052335..64054049-chr6:64060592..64063155,2	MCF-7	breast:
12	chr6:64057634..64059161-chr6:64281523..64283392,2	MCF-7	breast:
13	chr6:64091757..64094702-chr6:64282353..64283883,2	MCF-7	breast:
14	chr6:64048299..64050444-chr6:64282578..64285155,2	MCF-7	breast:
15	chr6:64061604..64062576-chr6:64512267..64512790,2	MCF-7	breast:
16	chr6:64061712..64062525-chr6:64473904..64474743,3	MCF-7	breast:
17	chr6:64080126..64083396-chr6:64281737..64284013,3	MCF-7	breast:
18	chr6:64061577..64062551-chr6:64473988..64474844,2	MCF-7	breast:
19	chr6:64062640..64063526-chr6:64474143..64474904,3	MCF-7	breast:
20	chr6:64078716..64081417-chr6:64082620..64086041,3	MCF-7	breast:
21	chr6:64078716..64081417-chr6:64082620..64086041,3	MCF-7	breast:
22	chr6:64079102..64081894-chr6:64099823..64102338,2	K562	blood:
23	chr6:64062812..64063338-chr6:64512230..64512915,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000218617	TF binding region
LGSN	TF binding region
ENSG00000218617	CpG island
LGSN	CpG island
ENSG00000266680	chromatin interactions
ENSG00000218617	chromatin interactions
ENSG00000112245	chromatin interactions

Extended variants
information (count: 3212 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3212 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7776434	chr6:64028392-64028393	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566156019	chr6:64028401-64028402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189132204	chr6:64028402-64028403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554327317	chr6:64028450-64028451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7752633	chr6:64028456-64028457	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs116786597	chr6:64028473-64028474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560067480	chr6:64028511-64028512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143426151	chr6:64028545-64028546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577074347	chr6:64028578-64028579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541014927	chr6:64028630-64028631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559133853	chr6:64028653-64028654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529795191	chr6:64028686-64028687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527322128	chr6:64028743-64028744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541978591	chr6:64028845-64028846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376715843	chr6:64028901-64028902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34315331	chr6:64028927-64028928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563386418	chr6:64028930-64028931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142514182	chr6:64028962-64028963	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs147523656	chr6:64029012-64029013	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs139407320	chr6:64029024-64029025	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs571870364	chr6:64029041-64029042	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs532736164	chr6:64029067-64029068	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs547767397	chr6:64029068-64029069	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs565974798	chr6:64029089-64029090	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs192044375	chr6:64029133-64029134	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs554615190	chr6:64029134-64029135	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs369177083	chr6:64029189-64029190	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs569816301	chr6:64029199-64029200	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs536807729	chr6:64029202-64029203	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs114762014	chr6:64029222-64029223	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs13212744	chr6:64029238-64029239	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs374477821	chr6:64029267-64029268	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs534636379	chr6:64029297-64029298	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs552920471	chr6:64029303-64029304	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs372603361	chr6:64029315-64029316	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs79223144	chr6:64029378-64029379	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs541870635	chr6:64029418-64029419	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs563327484	chr6:64029457-64029458	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs183993482	chr6:64029526-64029527	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs114682349	chr6:64029533-64029534	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs115610758	chr6:64029623-64029624	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs114226697	chr6:64029629-64029630	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs1711917	chr6:64029649-64029650	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs559640735	chr6:64029696-64029697	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs529989487	chr6:64029719-64029720	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs373324210	chr6:64029743-64029744	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs3778649	chr6:64029748-64029749	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs200879876	chr6:64029756-64029757	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs569803794	chr6:64029762-64029763	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs537192969	chr6:64029801-64029802	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	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	21364760	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164920	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64018200-64050800	Weak transcription	A549	lung
2	chr6:64027600-64028600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr6:64027600-64028600	Enhancers	Placenta Amnion	Placenta Amnion
4	chr6:64028200-64028600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr6:64028600-64029400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr6:64028600-64029800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr6:64029800-64030000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr6:64029800-64030000	Enhancers	Placenta Amnion	Placenta Amnion
9	chr6:64029800-64030200	Enhancers	Hela-S3	cervix
10	chr6:64030000-64031000	Enhancers	Fetal Brain Male	brain
11	chr6:64030400-64031000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:64031000-64032200	Weak transcription	Fetal Brain Male	brain
13	chr6:64032200-64034200	Enhancers	Fetal Brain Male	brain
14	chr6:64040400-64071200	Weak transcription	Placenta	Placenta
15	chr6:64043000-64043400	Enhancers	Stomach Mucosa	stomach
16	chr6:64050800-64053000	Strong transcription	A549	lung
17	chr6:64051000-64051400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr6:64051000-64051400	ZNF genes & repeats	Aorta	Aorta
19	chr6:64051000-64051400	Enhancers	Gastric	stomach
20	chr6:64051400-64058000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:64053000-64053800	Weak transcription	A549	lung
22	chr6:64053800-64054000	Strong transcription	A549	lung
23	chr6:64054000-64055600	Weak transcription	A549	lung
24	chr6:64055600-64056200	Strong transcription	A549	lung
25	chr6:64055800-64056600	Enhancers	Fetal Intestine Large	intestine
26	chr6:64056000-64056600	Enhancers	Fetal Intestine Small	intestine
27	chr6:64056000-64058200	Enhancers	HepG2	liver
28	chr6:64056200-64057200	Genic enhancers	A549	lung
29	chr6:64056600-64057000	Flanking Active TSS	Fetal Intestine Large	intestine
30	chr6:64056600-64057000	Flanking Active TSS	Fetal Intestine Small	intestine
31	chr6:64056600-64059800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr6:64056800-64059600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:64057000-64057600	Enhancers	Fetal Intestine Small	intestine
34	chr6:64057000-64058200	Active TSS	Fetal Intestine Large	intestine
35	chr6:64057000-64058400	Enhancers	NHLF	lung
36	chr6:64057000-64059200	Enhancers	NHEK	skin
37	chr6:64057000-64059600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:64057000-64059800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr6:64057200-64057400	Enhancers	A549	lung
40	chr6:64057200-64057600	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr6:64057200-64058400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr6:64057200-64059000	Enhancers	HMEC	breast
43	chr6:64057200-64059800	Enhancers	NHDF-Ad	bronchial
44	chr6:64057200-64060000	Enhancers	HUVEC	blood vessel
45	chr6:64057200-64062200	Enhancers	Hela-S3	cervix
46	chr6:64057400-64058000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr6:64057400-64058200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:64057400-64058200	Flanking Active TSS	A549	lung
49	chr6:64057400-64058200	Enhancers	NH-A	brain
50	chr6:64057400-64058200	Enhancers	Osteobl	bone

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