Variant report

Variant	nsv1031632
Chromosome Location	chr6:67196653-67833819
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2042)
CpG islands
(count:428)
Chromatin interactive
region (count:69)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2042 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:67206650-67206880	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:67772423-67772692	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:67776313-67776646	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:67199254-67199477	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:67719812-67720052	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:67774440-67774564	K562	blood:	n/a	n/a
7	ARID3A	chr6:67644267-67644467	K562	blood:	n/a	n/a
8	ARID3A	chr6:67772611-67773007	K562	blood:	n/a	n/a
9	ATF1	chr6:67610827-67611030	K562	blood:	n/a	n/a
10	ATF1	chr6:67723200-67723282	K562	blood:	n/a	n/a
11	BACH1	chr6:67429033-67429429	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr6:67719789-67719952	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr6:67776366-67776512	K562	blood:	n/a	n/a
14	BHLHE40	chr6:67544281-67544282	HepG2	liver:	n/a	n/a
15	BHLHE40	chr6:67719758-67720010	K562	blood:	n/a	n/a
16	BHLHE40	chr6:67620072-67620082	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:67606432-67606632	HepG2	liver:	n/a	n/a
18	BHLHE40	chr6:67719715-67720104	HepG2	liver:	n/a	n/a
19	BRCA1	chr6:67206671-67206866	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr6:67719810-67719996	HepG2	liver:	n/a	n/a
21	CBX3	chr6:67776315-67776639	K562	blood:	n/a	n/a
22	CBX3	chr6:67607501-67607759	K562	blood:	n/a	n/a
23	CBX3	chr6:67776351-67776637	K562	blood:	n/a	n/a
24	CCNT2	chr6:67446126-67446272	K562	blood:	n/a	n/a
25	CCNT2	chr6:67675300-67675575	K562	blood:	n/a	n/a
26	CCNT2	chr6:67257883-67258083	K562	blood:	n/a	n/a
27	CCNT2	chr6:67831789-67832133	K562	blood:	n/a	n/a
28	CEBPB	chr6:67445003-67445284	MCF-7	breast:	n/a	n/a
29	CEBPB	chr6:67658058-67658355	MCF-7	breast:	n/a	n/a
30	CEBPB	chr6:67641680-67641950	HepG2	liver:	n/a	chr6:67641780-67641793 chr6:67641777-67641794
31	CEBPB	chr6:67723581-67723882	HepG2	liver:	n/a	chr6:67723718-67723729
32	CEBPB	chr6:67564655-67564914	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:67338920-67339155	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr6:67658083-67658405	MCF-7	breast:	n/a	n/a
35	CEBPB	chr6:67199264-67199419	HepG2	liver:	n/a	n/a
36	CEBPB	chr6:67773444-67773779	K562	blood:	n/a	n/a
37	CEBPB	chr6:67607611-67607745	K562	blood:	n/a	n/a
38	CEBPB	chr6:67782365-67782600	HepG2	liver:	n/a	chr6:67782490-67782501
39	CEBPB	chr6:67795968-67796230	K562	blood:	n/a	chr6:67796118-67796129
40	CEBPB	chr6:67568046-67568371	MCF-7	breast:	n/a	chr6:67568283-67568294
41	CEBPB	chr6:67481436-67481915	HepG2	liver:	n/a	chr6:67481743-67481754
42	CEBPB	chr6:67812669-67813026	HepG2	liver:	n/a	chr6:67812853-67812864
43	CEBPB	chr6:67568149-67568413	H1-hESC	embryonic stem cell:	n/a	chr6:67568283-67568294
44	CEBPB	chr6:67481380-67481903	IMR90	lung:	n/a	chr6:67481743-67481754
45	CEBPB	chr6:67386720-67386956	HepG2	liver:	n/a	chr6:67386828-67386839
46	CEBPB	chr6:67607554-67607888	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:67812673-67813004	IMR90	lung:	n/a	chr6:67812853-67812864
48	CEBPB	chr6:67749035-67749107	K562	blood:	n/a	chr6:67749064-67749075 chr6:67749064-67749075
49	CEBPB	chr6:67568099-67568471	IMR90	lung:	n/a	chr6:67568283-67568294
50	CEBPB	chr6:67713777-67714033	MCF-7	breast:	n/a	chr6:67713935-67713946

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:67659187-67659237	ProgFib	skin:	n/a
2	chr6:67659187-67659237	ProgFib	skin:	n/a
3	chr6:67372805-67372855	HL-60	blood:	n/a
4	chr6:67741714-67741764	HMEC	breast:	n/a
5	chr6:67372805-67372855	Jurkat	blood:	n/a
6	chr6:67372805-67372855	HEEpiC	esophagus:	n/a
7	chr6:67659438-67659488	NB4	blood:	n/a
8	chr6:67658480-67658530	T-47D	breast:	n/a
9	chr6:67741651-67741701	ProgFib	skin:	n/a
10	chr6:67741651-67741701	AG09319	gingival:	n/a
11	chr6:67659187-67659237	AoSMC	blood vessel:	n/a
12	chr6:67659187-67659237	AG09319	gingival:	n/a
13	chr6:67659187-67659237	Jurkat	blood:	n/a
14	chr6:67659438-67659488	Jurkat	blood:	n/a
15	chr6:67658563-67658613	HNPCEpiC	eye:	n/a
16	chr6:67741651-67741701	HepG2	liver:	n/a
17	chr6:67741714-67741764	SK-N-SH_RA	brain:	n/a
18	chr6:67741714-67741764	AG04450	lung:	fetal
19	chr6:67741651-67741701	MCF10A-Er-Src	breast:	n/a
20	chr6:67372805-67372855	HMEC	breast:	n/a
21	chr6:67741714-67741764	NHDF-neo	bronchial:	n/a
22	chr6:67658563-67658613	U87	brain:	n/a
23	chr6:67741651-67741701	HAEpiC	amniotic membrane:	n/a
24	chr6:67741714-67741764	NT2-D1	testis:	n/a
25	chr6:67658480-67658530	NT2-D1	testis:	n/a
26	chr6:67658480-67658530	NH-A	brain:	n/a
27	chr6:67658563-67658613	HPAEpiC	pulmonary alveolar:	n/a
28	chr6:67658480-67658530	GM06990	blood:	n/a
29	chr6:67741714-67741764	NHBE	bronchial:	n/a
30	chr6:67741651-67741701	NT2-D1	testis:	n/a
31	chr6:67658563-67658613	A549	lung:	n/a
32	chr6:67659187-67659237	AG04449	skin:	fetal
33	chr6:67658480-67658530	HRPEpiC	eye:	n/a
34	chr6:67741651-67741701	NH-A	brain:	n/a
35	chr6:67659438-67659488	AG10803	skin:	n/a
36	chr6:67659187-67659237	Caco-2	colon:	n/a
37	chr6:67659438-67659488	SK-N-SH_RA	brain:	n/a
38	chr6:67372805-67372855	Caco-2	colon:	n/a
39	chr6:67659187-67659237	SKMC	muscle:	n/a
40	chr6:67658563-67658613	NB4	blood:	n/a
41	chr6:67658480-67658530	BJ	skin:	n/a
42	chr6:67659187-67659237	T-47D	breast:	n/a
43	chr6:67659187-67659237	HL-60	blood:	n/a
44	chr6:67658480-67658530	SK-N-SH_RA	brain:	n/a
45	chr6:67741714-67741764	SK-N-MC	brain:	n/a
46	chr6:67659438-67659488	GM12878	blood:	n/a
47	chr6:67658480-67658530	AG04450	lung:	fetal
48	chr6:67658480-67658530	HRCEpiC	kidney:	n/a
49	chr6:67659438-67659488	AG04450	lung:	fetal
50	chr6:67659438-67659488	ECC-1	luminal epithelium:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:67498200..67500094-chr6:67502511..67504222,2	K562	blood:
2	chr6:67731062..67733775-chr6:67734181..67735767,2	MCF-7	breast:
3	chr6:67437935..67440519-chr6:67450054..67451766,2	MCF-7	breast:
4	chr6:67395567..67397940-chr6:67398717..67401472,2	MCF-7	breast:
5	chr6:67778065..67781225-chr6:67782008..67784983,4	K562	blood:
6	chr6:67697416..67700217-chr6:67716740..67718720,2	K562	blood:
7	chr6:67774843..67776777-chr6:69022561..69024613,2	MCF-7	breast:
8	chr6:67796143..67796843-chr6:68573181..68573682,2	MCF-7	breast:
9	chr6:67697416..67700217-chr6:67716740..67718720,2	K562	blood:
10	chr6:67754608..67756147-chr6:67757015..67759750,2	MCF-7	breast:
11	chr6:67767080..67769379-chr6:67772486..67774394,2	K562	blood:
12	chr6:67636826..67639519-chr6:67639746..67642162,2	MCF-7	breast:
13	chr6:67444035..67445602-chr6:67467321..67470061,2	MCF-7	breast:
14	chr6:67731062..67733775-chr6:67734181..67735767,2	MCF-7	breast:
15	chr6:67388795..67391357-chr6:67397972..67399785,2	K562	blood:
16	chr6:67512172..67514345-chr6:67514772..67516688,2	MCF-7	breast:
17	chr6:67388795..67391357-chr6:67397972..67399785,2	K562	blood:
18	chr6:67703812..67706032-chr6:67716375..67719338,2	K562	blood:
19	chr6:67616212..67617756-chr6:67621376..67624095,2	MCF-7	breast:
20	chr6:67776186..67778175-chr6:67786497..67788108,2	K562	blood:
21	chr6:67690651..67692337-chr6:67701670..67703736,2	K562	blood:
22	chr6:67664280..67666953-chr6:67670600..67673248,2	MCF-7	breast:
23	chr6:67797177..67799198-chr6:67799977..67801822,2	K562	blood:
24	chr4:106066864..106069364-chr6:67678829..67681478,2	MCF-7	breast:
25	chr6:67754798..67756430-chr6:67760410..67762819,2	MCF-7	breast:
26	chr6:67782061..67786173-chr6:67786217..67792802,8	K562	blood:
27	chr6:67429289..67430062-chr7:148844726..148845241,2	MCF-7	breast:
28	chr6:67680520..67684153-chr6:67686504..67689501,3	MCF-7	breast:
29	chr6:67703812..67706032-chr6:67716375..67719338,2	K562	blood:
30	chr6:67779443..67782411-chr6:67785393..67788162,4	K562	blood:
31	chr6:67652736..67654313-chr6:67654518..67657198,2	MCF-7	breast:
32	chr6:67782061..67786173-chr6:67786217..67792802,8	K562	blood:
33	chr6:67628434..67630192-chr6:67648108..67650563,2	K562	blood:
34	chr6:67444035..67445602-chr6:67467321..67470061,2	MCF-7	breast:
35	chr6:67664280..67666953-chr6:67670600..67673248,2	MCF-7	breast:
36	chr6:67767080..67769379-chr6:67772486..67774394,2	K562	blood:
37	chr6:67616212..67617756-chr6:67621376..67624095,2	MCF-7	breast:
38	chr6:67783004..67786159-chr6:67787646..67791458,3	K562	blood:
39	chr6:67531677..67533488-chr6:67538061..67540928,2	K562	blood:
40	chr6:67797177..67799198-chr6:67799977..67801822,2	K562	blood:
41	chr6:67534211..67536445-chr6:67538569..67540725,2	MCF-7	breast:
42	chr6:67776186..67778175-chr6:67786497..67788108,2	K562	blood:
43	chr6:67660837..67662514-chr6:67666593..67669025,2	MCF-7	breast:
44	chr6:67660837..67662514-chr6:67666593..67669025,2	MCF-7	breast:
45	chr5:101725894..101726537-chr6:67534604..67535331,2	MCF-7	breast:
46	chr6:67641579..67644100-chr6:68068975..68070914,2	K562	blood:
47	chr6:67636826..67639519-chr6:67639746..67642162,2	MCF-7	breast:
48	chr6:67779443..67782411-chr6:67785393..67788162,4	K562	blood:
49	chr12:47503984..47504568-chr6:67484757..67485277,2	MCF-7	breast:
50	chr6:67498200..67500094-chr6:67502511..67504222,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EYS-5	chr6:67420135-67420720	NONHSAT113381

No data

Variant related genes	Relation type
RNU7-66P	TF binding region
ENSG00000270521	TF binding region
RNU7-66P	CpG island
ENSG00000270521	CpG island
ENSG00000238949	chromatin interactions
ENSG00000197024	chromatin interactions
ENSG00000168769	chromatin interactions

Extended variants
information (count: 5493 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:5493 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537699232	chr6:67198802-67198803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372598341	chr6:67198815-67198816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186357368	chr6:67198843-67198844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377043370	chr6:67198848-67198849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191262325	chr6:67198873-67198874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539462345	chr6:67198875-67198876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs565077024	chr6:67198877-67198878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553414838	chr6:67198881-67198882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573282369	chr6:67198887-67198888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11754369	chr6:67198893-67198894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540825997	chr6:67198928-67198929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183466099	chr6:67198948-67198949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574303849	chr6:67198960-67198961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs62417263	chr6:67198983-67198984	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs138843645	chr6:67199072-67199073	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs532098324	chr6:67199083-67199084	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs62417264	chr6:67199084-67199085	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs112340097	chr6:67199086-67199087	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs528235026	chr6:67199090-67199091	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs62417265	chr6:67199091-67199092	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs113140603	chr6:67199148-67199149	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs368935451	chr6:67199161-67199162	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs568622485	chr6:67199176-67199177	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs537663853	chr6:67199178-67199179	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs62417266	chr6:67199181-67199182	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs571091576	chr6:67199183-67199184	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs11754444	chr6:67199184-67199185	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs553140196	chr6:67199194-67199195	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs532649947	chr6:67199264-67199265	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs373163851	chr6:67199276-67199277	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs571628120	chr6:67199281-67199282	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs535516721	chr6:67199286-67199287	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs555444213	chr6:67199337-67199338	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs79527922	chr6:67199342-67199343	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs75279861	chr6:67199359-67199360	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs557207324	chr6:67199360-67199361	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs2812174	chr6:67199382-67199383	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs116566192	chr6:67199427-67199428	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs569445974	chr6:67199448-67199449	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs545773306	chr6:67199468-67199469	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs376782281	chr6:67199480-67199481	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs113491128	chr6:67199493-67199494	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs112701802	chr6:67199521-67199522	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs62417267	chr6:67199522-67199523	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs187543621	chr6:67199523-67199524	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs111465088	chr6:67199552-67199553	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs114956975	chr6:67199558-67199559	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs561782405	chr6:67199595-67199596	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs537491023	chr6:67199643-67199644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140453240	chr6:67199651-67199652	Enhancers	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
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
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	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	21364760	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	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
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Obesity	20950786	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:67198800-67199000	Enhancers	HepG2	liver
2	chr6:67199000-67199600	Flanking Active TSS	HepG2	liver
3	chr6:67199600-67200000	Enhancers	HepG2	liver
4	chr6:67216800-67217200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr6:67217000-67217200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr6:67217200-67218200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr6:67217200-67218200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr6:67218000-67218800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr6:67218000-67219600	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr6:67218200-67218600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr6:67218200-67218600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:67218200-67218600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:67218200-67218600	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr6:67218200-67218600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:67218200-67218800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:67218200-67218800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr6:67218200-67218800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:67218200-67218800	Enhancers	NH-A	brain
19	chr6:67218600-67219400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:67219400-67219600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr6:67224400-67224800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr6:67224800-67228200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr6:67228200-67229200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr6:67228200-67229200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr6:67228400-67228800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:67228400-67229200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr6:67243200-67244400	Enhancers	Primary hematopoietic stem cells	blood
28	chr6:67243200-67244400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:67244400-67247400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:67244600-67246000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:67245400-67246600	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr6:67245600-67245800	Enhancers	Duodenum Mucosa	Duodenum
33	chr6:67245600-67246200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:67245600-67246800	Enhancers	Brain Germinal Matrix	brain
35	chr6:67246600-67248400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr6:67246800-67248800	Weak transcription	Brain Germinal Matrix	brain
37	chr6:67247400-67248200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:67248000-67249000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:67248200-67248800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr6:67248400-67249200	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr6:67248400-67249200	Enhancers	Brain Hippocampus Middle	brain
42	chr6:67248400-67249200	Enhancers	Brain Substantia Nigra	brain
43	chr6:67248600-67249000	Enhancers	Fetal Lung	lung
44	chr6:67248800-67249000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:67248800-67249200	Enhancers	Brain Germinal Matrix	brain
46	chr6:67266200-67266600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr6:67272800-67273200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr6:67273200-67273800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr6:67273600-67273800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr6:67281200-67281800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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