Variant report

Variant	nsv1031548
Chromosome Location	chr6:64026862-64102045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:827)
CpG islands
(count:185)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:827 , 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	chr6:64058006-64058016	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:64101330-64101949	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:64061842-64062271	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:64062913-64063349	HepG2	liver:	n/a	n/a
5	ATF1	chr6:64083127-64083308	K562	blood:	n/a	n/a
6	ATF2	chr6:64061990-64063362	GM12878	blood:	n/a	n/a
7	ATF2	chr6:64057519-64057901	GM12878	blood:	n/a	n/a
8	ATF2	chr6:64062307-64063405	GM12878	blood:	n/a	n/a
9	ATF3	chr6:64062702-64063222	GM12878	blood:	n/a	n/a
10	BATF	chr6:64057524-64057796	GM12878	blood:	n/a	n/a
11	BATF	chr6:64086526-64086830	GM12878	blood:	n/a	chr6:64086675-64086686
12	BATF	chr6:64057503-64057905	GM12878	blood:	n/a	n/a
13	BATF	chr6:64062394-64062984	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	chr6:64062213-64063430	GM12878	blood:	n/a	n/a
18	BCLAF1	chr6:64062312-64063311	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:64101403-64101854	HepG2	liver:	n/a	n/a
20	BHLHE40	chr6:64093740-64094165	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:64061987-64063282	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	chr6:64072861-64072981	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:64101389-64101791	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:64065437-64065832	Hela-S3	cervix:	n/a	chr6:64065639-64065650
29	CEBPB	chr6:64062474-64063043	GM12878	blood:	n/a	n/a
30	CEBPB	chr6:64065537-64065723	HepG2	liver:	n/a	chr6:64065639-64065650
31	CEBPB	chr6:64065498-64065825	A549	lung:	n/a	chr6:64065639-64065650
32	CEBPB	chr6:64062990-64063317	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:64065512-64065808	A549	lung:	n/a	chr6:64065639-64065650
34	CEBPB	chr6:64057333-64058060	HCT-116	colon:	n/a	chr6:64057610-64057622
35	CEBPB	chr6:64065399-64065779	MCF-7	breast:	n/a	chr6:64065639-64065650
36	CEBPB	chr6:64061923-64062415	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr6:64065562-64065813	HepG2	liver:	n/a	chr6:64065639-64065650
38	CEBPB	chr6:64101370-64101827	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:64062286-64063500	GM12878	blood:	n/a	n/a
40	CEBPB	chr6:64098031-64098201	A549	lung:	n/a	chr6:64098116-64098125 chr6:64098116-64098125
41	CEBPB	chr6:64098075-64098264	HepG2	liver:	n/a	chr6:64098116-64098125 chr6:64098116-64098125
42	CEBPB	chr6:64057464-64057979	A549	lung:	n/a	chr6:64057610-64057622
43	CEBPB	chr6:64065384-64065879	A549	lung:	n/a	chr6:64065639-64065650
44	CEBPB	chr6:64062632-64063362	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr6:64062460-64063288	GM12878	blood:	n/a	n/a
46	CHD2	chr6:64065435-64065635	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr6:64093731-64094180	GM12878	blood:	n/a	n/a
48	CTCF	chr6:64061800-64062204	MCF-7	breast:	n/a	chr6:64062055-64062076 chr6:64062053-64062071 chr6:64062054-64062070
49	CTCF	chr6:64061980-64062130	RPTEC	kidney:	n/a	chr6:64062055-64062076 chr6:64062053-64062071 chr6:64062054-64062070
50	CTCF	chr6:64061861-64062297	GM12878	blood:	n/a	chr6:64062055-64062076 chr6:64062053-64062071 chr6:64062054-64062070

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:64029870-64029920	SKMC	muscle:	n/a
2	chr6:64029870-64029920	HRPEpiC	eye:	n/a
3	chr6:64029870-64029920	SKMC	muscle:	n/a
4	chr6:64029870-64029920	HRPEpiC	eye:	n/a
5	chr6:64042706-64042756	GM06990	blood:	n/a
6	chr6:64042706-64042756	HAEpiC	amniotic membrane:	n/a
7	chr6:64029870-64029920	ECC-1	luminal epithelium:	n/a
8	chr6:64042706-64042756	ProgFib	skin:	n/a
9	chr6:64029870-64029920	SAEC	small airway:	n/a
10	chr6:64042706-64042756	Jurkat	blood:	n/a
11	chr6:64042706-64042756	HCF	heart:	n/a
12	chr6:64029870-64029920	HEEpiC	esophagus:	n/a
13	chr6:64029870-64029920	AG04450	lung:	fetal
14	chr6:64042706-64042756	SAEC	small airway:	n/a
15	chr6:64042706-64042756	AG04450	lung:	fetal
16	chr6:64029870-64029920	ovcar-3	ovarian:	n/a
17	chr6:64029870-64029920	AG10803	skin:	n/a
18	chr6:64030429-64030479	AG04450	lung:	fetal
19	chr6:64030429-64030479	HNPCEpiC	eye:	n/a
20	chr6:64030429-64030479	LNCaP	prostate:	n/a
21	chr6:64042706-64042756	HRCEpiC	kidney:	n/a
22	chr6:64030429-64030479	SK-N-SH	brain:	n/a
23	chr6:64030429-64030479	Hela-S3	cervix:	n/a
24	chr6:64029870-64029920	PFSK-1	brain:	n/a
25	chr6:64030429-64030479	HEK293	kidney:	embryo
26	chr6:64030429-64030479	AoSMC	blood vessel:	n/a
27	chr6:64029870-64029920	A549	lung:	n/a
28	chr6:64042706-64042756	K562	blood:	n/a
29	chr6:64042706-64042756	H1-hESC	embryonic stem cell:	embryo
30	chr6:64030429-64030479	GM12891	blood:	n/a
31	chr6:64029870-64029920	H1-hESC	embryonic stem cell:	embryo
32	chr6:64029870-64029920	GM12892	blood:	n/a
33	chr6:64029870-64029920	AG09309	skin:	n/a
34	chr6:64029870-64029920	BJ	skin:	n/a
35	chr6:64029870-64029920	CMK	blood:	n/a
36	chr6:64042706-64042756	RPTEC	kidney:	n/a
37	chr6:64029870-64029920	ProgFib	skin:	n/a
38	chr6:64042706-64042756	ECC-1	luminal epithelium:	n/a
39	chr6:64030429-64030479	K562	blood:	n/a
40	chr6:64042706-64042756	AG04449	skin:	fetal
41	chr6:64030429-64030479	AG09319	gingival:	n/a
42	chr6:64030429-64030479	Jurkat	blood:	n/a
43	chr6:64030429-64030479	GM12878	blood:	n/a
44	chr6:64042706-64042756	Caco-2	colon:	n/a
45	chr6:64029870-64029920	HepG2	liver:	n/a
46	chr6:64030429-64030479	PrEC	prostate:	n/a
47	chr6:64029870-64029920	PrEC	prostate:	n/a
48	chr6:64030429-64030479	ProgFib	skin:	n/a
49	chr6:64042706-64042756	AG09309	skin:	n/a
50	chr6:64029870-64029920	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr6:64078716..64081417-chr6:64082620..64086041,3	MCF-7	breast:
2	chr6:64078716..64081417-chr6:64082620..64086041,3	MCF-7	breast:
3	chr6:64080126..64083396-chr6:64281737..64284013,3	MCF-7	breast:
4	chr6:64061851..64067000-chr6:64282014..64286349,7	MCF-7	breast:
5	chr6:64060326..64062411-chr6:64092797..64095365,2	K562	blood:
6	chr6:64062640..64063526-chr6:64474143..64474904,3	MCF-7	breast:
7	chr6:64062641..64063566-chr6:64308201..64309203,4	MCF-7	breast:
8	chr6:64028950..64031387-chr6:64282272..64283955,2	MCF-7	breast:
9	chr6:64060326..64062411-chr6:64092797..64095365,2	K562	blood:
10	chr6:64061577..64062551-chr6:64473988..64474844,2	MCF-7	breast:
11	chr6:64059286..64067591-chr6:64279675..64285580,14	MCF-7	breast:
12	chr6:64048299..64050444-chr6:64282578..64285155,2	MCF-7	breast:
13	chr6:64061712..64062525-chr6:64473904..64474743,3	MCF-7	breast:
14	chr6:64061604..64062576-chr6:64512267..64512790,2	MCF-7	breast:
15	chr6:64052335..64054049-chr6:64060592..64063155,2	MCF-7	breast:
16	chr6:64091757..64094702-chr6:64282353..64283883,2	MCF-7	breast:
17	chr6:64079102..64081894-chr6:64099823..64102338,2	K562	blood:
18	chr6:64057634..64059161-chr6:64281523..64283392,2	MCF-7	breast:
19	chr6:64062103..64065068-chr6:64510364..64512443,2	MCF-7	breast:
20	chr6:64062812..64063338-chr6:64512230..64512915,2	MCF-7	breast:
21	chr6:64052335..64054049-chr6:64060592..64063155,2	MCF-7	breast:
22	chr6:64082531..64084931-chr6:64282447..64284673,2	MCF-7	breast:
23	chr6:64062639..64063365-chr6:64283555..64284772,4	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: 3275 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3275 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549292552	chr6:64026876-64026877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181359281	chr6:64026935-64026936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572407827	chr6:64027073-64027074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142923739	chr6:64027137-64027138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549369294	chr6:64027159-64027160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185288531	chr6:64027171-64027172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs151101488	chr6:64027243-64027244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530358160	chr6:64027323-64027324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551662141	chr6:64027335-64027336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140986641	chr6:64027348-64027349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115110720	chr6:64027379-64027380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73761820	chr6:64027405-64027406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556069669	chr6:64027416-64027417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143736565	chr6:64027517-64027518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189743533	chr6:64027610-64027611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556638453	chr6:64027616-64027617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558272268	chr6:64027619-64027620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576104670	chr6:64027640-64027641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546713900	chr6:64027644-64027645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545509917	chr6:64027645-64027646	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543481346	chr6:64027655-64027656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368640630	chr6:64027676-64027677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146781113	chr6:64027703-64027704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560802836	chr6:64027728-64027729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531511343	chr6:64027737-64027738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7750464	chr6:64027800-64027801	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs564567546	chr6:64027803-64027804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12111559	chr6:64027808-64027809	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs140535051	chr6:64027848-64027849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561961740	chr6:64027874-64027875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145525285	chr6:64027875-64027876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529404883	chr6:64027879-64027880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534357818	chr6:64027892-64027893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7775614	chr6:64027911-64027912	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs567953085	chr6:64027923-64027924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148909557	chr6:64027942-64027943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373777148	chr6:64027944-64027945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139994016	chr6:64027949-64027950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77867605	chr6:64028016-64028017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7751985	chr6:64028047-64028048	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs138093576	chr6:64028054-64028055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7750847	chr6:64028055-64028056	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs554209204	chr6:64028060-64028061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12111159	chr6:64028066-64028067	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs182085594	chr6:64028067-64028068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560789165	chr6:64028074-64028075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535328707	chr6:64028077-64028078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555249633	chr6:64028085-64028086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575910530	chr6:64028130-64028131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79942209	chr6:64028174-64028175	Enhancers Weak transcription	n/a	n/a	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:309 , 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	chr6:64024400-64027600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr6:64027600-64028600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr6:64027600-64028600	Enhancers	Placenta Amnion	Placenta Amnion
5	chr6:64028200-64028600	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr6:64028600-64029400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr6:64028600-64029800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr6:64029800-64030000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr6:64029800-64030000	Enhancers	Placenta Amnion	Placenta Amnion
10	chr6:64029800-64030200	Enhancers	Hela-S3	cervix
11	chr6:64030000-64031000	Enhancers	Fetal Brain Male	brain
12	chr6:64030400-64031000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:64031000-64032200	Weak transcription	Fetal Brain Male	brain
14	chr6:64032200-64034200	Enhancers	Fetal Brain Male	brain
15	chr6:64040400-64071200	Weak transcription	Placenta	Placenta
16	chr6:64043000-64043400	Enhancers	Stomach Mucosa	stomach
17	chr6:64050800-64053000	Strong transcription	A549	lung
18	chr6:64051000-64051400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:64051000-64051400	ZNF genes & repeats	Aorta	Aorta
20	chr6:64051000-64051400	Enhancers	Gastric	stomach
21	chr6:64051400-64058000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:64053000-64053800	Weak transcription	A549	lung
23	chr6:64053800-64054000	Strong transcription	A549	lung
24	chr6:64054000-64055600	Weak transcription	A549	lung
25	chr6:64055600-64056200	Strong transcription	A549	lung
26	chr6:64055800-64056600	Enhancers	Fetal Intestine Large	intestine
27	chr6:64056000-64056600	Enhancers	Fetal Intestine Small	intestine
28	chr6:64056000-64058200	Enhancers	HepG2	liver
29	chr6:64056200-64057200	Genic enhancers	A549	lung
30	chr6:64056600-64057000	Flanking Active TSS	Fetal Intestine Large	intestine
31	chr6:64056600-64057000	Flanking Active TSS	Fetal Intestine Small	intestine
32	chr6:64056600-64059800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:64056800-64059600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:64057000-64057600	Enhancers	Fetal Intestine Small	intestine
35	chr6:64057000-64058200	Active TSS	Fetal Intestine Large	intestine
36	chr6:64057000-64058400	Enhancers	NHLF	lung
37	chr6:64057000-64059200	Enhancers	NHEK	skin
38	chr6:64057000-64059600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr6:64057000-64059800	Enhancers	Muscle Satellite Cultured Cells	--
40	chr6:64057200-64057400	Enhancers	A549	lung
41	chr6:64057200-64057600	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr6:64057200-64058400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr6:64057200-64059000	Enhancers	HMEC	breast
44	chr6:64057200-64059800	Enhancers	NHDF-Ad	bronchial
45	chr6:64057200-64060000	Enhancers	HUVEC	blood vessel
46	chr6:64057200-64062200	Enhancers	Hela-S3	cervix
47	chr6:64057400-64058000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr6:64057400-64058200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:64057400-64058200	Flanking Active TSS	A549	lung
50	chr6:64057400-64058200	Enhancers	NH-A	brain

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