Variant report

Variant	nsv5449
Chromosome Location	chr6:117954646-117999751
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:922)
CpG islands
(count:918)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:922 , 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	chr6:117995784-117996651	K562	blood:	n/a	n/a
2	ARID3A	chr6:117996172-117996692	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:117998708-117999094	K562	blood:	n/a	n/a
4	ARID3A	chr6:117976093-117976135	K562	blood:	n/a	n/a
5	ARID3A	chr6:117974951-117975573	K562	blood:	n/a	n/a
6	ATF1	chr6:117974892-117975454	K562	blood:	n/a	n/a
7	ATF1	chr6:117996388-117996779	K562	blood:	n/a	n/a
8	ATF1	chr6:117998675-117999071	K562	blood:	n/a	n/a
9	ATF2	chr6:117996053-117996784	GM12878	blood:	n/a	n/a
10	ATF2	chr6:117996252-117996701	GM12878	blood:	n/a	n/a
11	ATF2	chr6:117996133-117996640	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr6:117996234-117996641	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr6:117996283-117996656	K562	blood:	n/a	chr6:117996491-117996511 chr6:117996640-117996649
14	BACH1	chr6:117989103-117989104	K562	blood:	n/a	n/a
15	BACH1	chr6:117996262-117996689	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr6:117996799-117997166	GM12878	blood:	n/a	n/a
17	BATF	chr6:117996318-117996638	GM12878	blood:	n/a	n/a
18	BATF	chr6:117997202-117997439	GM12878	blood:	n/a	n/a
19	BCL3	chr6:117996210-117996733	A549	lung:	n/a	chr6:117996672-117996681 chr6:117996722-117996731
20	BCLAF1	chr6:117996217-117996679	K562	blood:	n/a	n/a
21	BCLAF1	chr6:117996006-117996660	GM12878	blood:	n/a	n/a
22	BCLAF1	chr6:117975078-117975476	K562	blood:	n/a	n/a
23	BCLAF1	chr6:117996148-117996681	K562	blood:	n/a	chr6:117996672-117996681
24	BCLAF1	chr6:117996151-117996667	GM12878	blood:	n/a	n/a
25	BHLHE40	chr6:117995800-117996692	K562	blood:	n/a	n/a
26	BHLHE40	chr6:117996240-117996735	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:117997290-117997475	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:117975203-117975509	K562	blood:	n/a	n/a
29	BHLHE40	chr6:117993767-117994085	K562	blood:	n/a	n/a
30	BHLHE40	chr6:117996243-117996711	HepG2	liver:	n/a	n/a
31	BHLHE40	chr6:117997272-117997335	K562	blood:	n/a	n/a
32	BRCA1	chr6:117996265-117996544	HepG2	liver:	n/a	n/a
33	BRCA1	chr6:117996077-117996587	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr6:117996379-117996549	GM12878	blood:	n/a	n/a
35	BRCA1	chr6:117996313-117996667	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr6:117996188-117996695	K562	blood:	n/a	n/a
37	CBX3	chr6:117996124-117996855	HCT-116	colon:	n/a	n/a
38	CBX3	chr6:117997793-117998304	K562	blood:	n/a	n/a
39	CBX3	chr6:117995750-117996790	K562	blood:	n/a	n/a
40	CBX3	chr6:117974935-117975575	K562	blood:	n/a	n/a
41	CCNT2	chr6:117975027-117975390	K562	blood:	n/a	n/a
42	CCNT2	chr6:117996330-117996699	K562	blood:	n/a	chr6:117996640-117996649
43	CEBPB	chr6:117976035-117976319	HepG2	liver:	n/a	chr6:117976149-117976162 chr6:117976151-117976162 chr6:117976149-117976162 chr6:117976149-117976160
44	CEBPB	chr6:117995732-117996511	K562	blood:	n/a	chr6:117996065-117996078 chr6:117996066-117996077
45	CEBPB	chr6:117998809-117999309	HepG2	liver:	n/a	chr6:117999057-117999070
46	CEBPB	chr6:117998784-117999242	MCF-7	breast:	n/a	chr6:117999057-117999070
47	CEBPB	chr6:117995916-117996230	IMR90	lung:	n/a	chr6:117996065-117996078 chr6:117996066-117996077
48	CEBPB	chr6:117975965-117976343	K562	blood:	n/a	chr6:117976149-117976162 chr6:117976151-117976162 chr6:117976149-117976162 chr6:117976149-117976160
49	CEBPB	chr6:117998910-117999058	K562	blood:	n/a	n/a
50	CEBPB	chr6:117958981-117959561	HepG2	liver:	n/a	chr6:117959404-117959415

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:117995843-117995893	SAEC	small airway:	n/a
2	chr6:117993457-117993507	GM19239	blood:	n/a
3	chr6:117996486-117996536	H1-hESC	embryonic stem cell:	embryo
4	chr6:117995843-117995893	SAEC	small airway:	n/a
5	chr6:117993457-117993507	GM19239	blood:	n/a
6	chr6:117996486-117996536	H1-hESC	embryonic stem cell:	embryo
7	chr6:117996645-117996695	MCF-7	breast:	n/a
8	chr6:117996414-117996464	ovcar-3	ovarian:	n/a
9	chr6:117995843-117995893	ECC-1	luminal epithelium:	n/a
10	chr6:117995843-117995893	LNCaP	prostate:	n/a
11	chr6:117996421-117996471	Caco-2	colon:	n/a
12	chr6:117996341-117996391	SK-N-SH_RA	brain:	n/a
13	chr6:117996341-117996391	BE2_C	brain:	n/a
14	chr6:117997284-117997334	BE2_C	brain:	n/a
15	chr6:117996421-117996471	SKMC	muscle:	n/a
16	chr6:117993457-117993507	AG04449	skin:	fetal
17	chr6:117997374-117997424	HAEpiC	amniotic membrane:	n/a
18	chr6:117996544-117996594	AG09319	gingival:	n/a
19	chr6:117996341-117996391	SAEC	small airway:	n/a
20	chr6:117996341-117996391	HRCEpiC	kidney:	n/a
21	chr6:117993457-117993507	MCF-7	breast:	n/a
22	chr6:117993457-117993507	HepG2	liver:	n/a
23	chr6:117995812-117995862	GM06990	blood:	n/a
24	chr6:117996486-117996536	HNPCEpiC	eye:	n/a
25	chr6:117996486-117996536	PrEC	prostate:	n/a
26	chr6:117997374-117997424	RPTEC	kidney:	n/a
27	chr6:117996435-117996485	HRE	kidney:	n/a
28	chr6:117996399-117996449	SAEC	small airway:	n/a
29	chr6:117995843-117995893	HCT-116	colon:	n/a
30	chr6:117996421-117996471	CMK	blood:	n/a
31	chr6:117993457-117993507	GM12891	blood:	n/a
32	chr6:117996544-117996594	AG04450	lung:	fetal
33	chr6:117996645-117996695	GM12891	blood:	n/a
34	chr6:117996414-117996464	SKMC	muscle:	n/a
35	chr6:117996399-117996449	HEEpiC	esophagus:	n/a
36	chr6:117997284-117997334	SK-N-SH	brain:	n/a
37	chr6:117996645-117996695	U87	brain:	n/a
38	chr6:117996645-117996695	SAEC	small airway:	n/a
39	chr6:117995812-117995862	HIPEpiC	eye:	n/a
40	chr6:117996544-117996594	GM12891	blood:	n/a
41	chr6:117995812-117995862	HAEpiC	amniotic membrane:	n/a
42	chr6:117996470-117996520	GM06990	blood:	n/a
43	chr6:117996399-117996449	LNCaP	prostate:	n/a
44	chr6:117996486-117996536	NT2-D1	testis:	n/a
45	chr6:117996421-117996471	T-47D	breast:	n/a
46	chr6:117996414-117996464	HEK293	kidney:	embryo
47	chr6:117997374-117997424	HEK293	kidney:	embryo
48	chr6:117997374-117997424	PANC-1	pancreas:	n/a
49	chr6:117996486-117996536	BE2_C	brain:	n/a
50	chr6:117996435-117996485	RPTEC	kidney:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:117919854..117927630-chr6:117992313..117999313,9	K562	blood:
2	chr6:117922238..117925071-chr6:117951173..117954790,3	K562	blood:
3	chr6:117989002..117991438-chr6:117994299..117996624,2	K562	blood:
4	chr6:117951506..117953445-chr6:117960272..117964115,3	K562	blood:
5	chr6:117954014..117956876-chr6:117960309..117961925,2	K562	blood:
6	chr6:117986656..117990988-chr6:117991172..117993909,4	K562	blood:
7	chr6:117976462..117978203-chr6:117993552..117995244,2	K562	blood:
8	chr6:117919537..117925760-chr6:117993513..117997816,10	K562	blood:
9	chr6:117976380..117977960-chr6:117980811..117982683,2	MCF-7	breast:
10	chr6:117975355..117979268-chr6:117992487..117995744,5	K562	blood:
11	chr6:117745008..117746813-chr6:117997371..118000151,2	MCF-7	breast:
12	chr6:117989002..117991438-chr6:117994299..117996624,2	K562	blood:
13	chr6:117976462..117978203-chr6:117993552..117995244,2	K562	blood:
14	chr6:117976607..117978238-chr6:117987191..117988700,2	K562	blood:
15	chr6:117922178..117924221-chr6:117997147..117999615,2	MCF-7	breast:
16	chr6:117976380..117977960-chr6:117980811..117982683,2	MCF-7	breast:
17	chr6:117921339..117924676-chr6:117954310..117957194,3	MCF-7	breast:
18	chr6:117991023..117993739-chr6:117994900..117997573,2	K562	blood:
19	chr6:117921314..117923710-chr6:117975596..117977707,2	K562	blood:
20	chr6:117976607..117978238-chr6:117987191..117988700,2	K562	blood:
21	chr6:117764099..117766879-chr6:117995038..117997863,2	MCF-7	breast:
22	chr6:117922027..117923710-chr6:117974781..117977096,2	K562	blood:
23	chr6:117988434..117990727-chr6:117995010..117997280,2	K562	blood:
24	chr6:117962591..117965580-chr6:117994482..117996305,2	K562	blood:
25	chr6:117975355..117979268-chr6:117992487..117995744,5	K562	blood:
26	chr6:117962591..117965580-chr6:117994482..117996305,2	K562	blood:
27	chr6:117986656..117990988-chr6:117991172..117993909,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUS1-1	chr6:117974549-117975592	NONHSAT114684
2	lnc-NUS1-2	chr6:117973393-117974451	NONHSAT114683

No data

Variant related genes	Relation type
NUS1	TF binding region
NEPNP	TF binding region
NUS1	CpG island
NEPNP	CpG island
ENSG00000047932	chromatin interactions
ENSG00000221434	chromatin interactions
ENSG00000153989	chromatin interactions
ENSG00000218233	chromatin interactions

Extended variants
information (count: 1610 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:1610 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188718114	chr6:117954693-117954694	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs193220209	chr6:117954709-117954710	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143676059	chr6:117954729-117954730	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs371987966	chr6:117954730-117954731	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551031418	chr6:117954731-117954732	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566456440	chr6:117954759-117954760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs114728642	chr6:117954781-117954782	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs555070278	chr6:117954824-117954825	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs115717009	chr6:117954828-117954829	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536193328	chr6:117954849-117954850	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs557572861	chr6:117954883-117954884	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185641898	chr6:117954920-117954921	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs551685394	chr6:117954933-117954934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs539383792	chr6:117954942-117954943	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs546436004	chr6:117954968-117954969	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs564564387	chr6:117955003-117955004	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572509666	chr6:117955067-117955068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs17818735	chr6:117955078-117955079	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs540621498	chr6:117955119-117955120	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561219403	chr6:117955195-117955196	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs111860391	chr6:117955213-117955214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9374674	chr6:117955214-117955215	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs550491633	chr6:117955277-117955278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs180918222	chr6:117955282-117955283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs532925653	chr6:117955285-117955286	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs147180352	chr6:117955287-117955288	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78549702	chr6:117955293-117955294	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs527440898	chr6:117955389-117955390	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548952941	chr6:117955391-117955392	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs117442721	chr6:117955475-117955476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs28522156	chr6:117955487-117955488	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs17079404	chr6:117955518-117955519	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs569581359	chr6:117955519-117955520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565131060	chr6:117955535-117955536	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184145373	chr6:117955540-117955541	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs17079406	chr6:117955601-117955602	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs375472437	chr6:117955610-117955611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558116169	chr6:117955657-117955658	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs139149969	chr6:117955658-117955659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547532110	chr6:117955663-117955664	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs367897386	chr6:117955679-117955680	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs371710320	chr6:117955692-117955693	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs372541624	chr6:117955697-117955698	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs188867478	chr6:117955734-117955735	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573673410	chr6:117955737-117955738	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs4946272	chr6:117955740-117955741	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs562400908	chr6:117955742-117955743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs533059125	chr6:117955745-117955746	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs544800349	chr6:117955778-117955779	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs560128846	chr6:117955802-117955803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
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
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:745 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117950800-117975000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:117955400-117960000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr6:117957800-117961000	Weak transcription	K562	blood
4	chr6:117958800-117959800	Enhancers	HepG2	liver
5	chr6:117959400-117959800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
6	chr6:117959800-117960800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr6:117960800-117961600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
8	chr6:117961000-117961400	ZNF genes & repeats	K562	blood
9	chr6:117961400-117966600	Weak transcription	K562	blood
10	chr6:117961600-117981800	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr6:117962200-117985400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr6:117963400-117981800	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr6:117964600-117965000	Enhancers	Fetal Brain Male	brain
14	chr6:117965200-117967800	Weak transcription	Gastric	stomach
15	chr6:117965800-117966800	Weak transcription	Psoas Muscle	Psoas
16	chr6:117966600-117967000	Enhancers	K562	blood
17	chr6:117967000-117974800	Weak transcription	K562	blood
18	chr6:117969400-117995800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr6:117971800-117989800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr6:117973000-117990600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr6:117973800-117995600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr6:117974800-117975200	Flanking Active TSS	K562	blood
23	chr6:117975000-117975200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:117975200-117975600	Enhancers	Thymus	Thymus
25	chr6:117975200-117976600	Enhancers	K562	blood
26	chr6:117975200-117979800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:117975600-117976000	Weak transcription	Thymus	Thymus
28	chr6:117975600-117986200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr6:117976000-117977000	Enhancers	Thymus	Thymus
30	chr6:117976000-117977400	Enhancers	Fetal Thymus	thymus
31	chr6:117976200-117977000	Enhancers	Dnd41	blood
32	chr6:117976200-117977600	Enhancers	Primary T cells from cord blood	blood
33	chr6:117976400-117977000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr6:117976400-117977000	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr6:117976400-117977400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr6:117976600-117986400	Weak transcription	K562	blood
37	chr6:117978000-117995600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:117979400-117985600	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr6:117979800-117980200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:117980200-117981200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:117980800-117985600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr6:117981200-117983000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr6:117981800-117982600	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr6:117981800-117983000	Strong transcription	H1 Cell Line	embryonic stem cell
45	chr6:117982600-117990000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr6:117983000-117983400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr6:117983000-117983400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr6:117983400-117984600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr6:117983400-117984800	Strong transcription	H1 Cell Line	embryonic stem cell
50	chr6:117984600-117991000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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