Variant report

Variant	nsv1026532
Chromosome Location	chr6:35502604-35568562
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1123)
CpG islands
(count:550)
Chromatin interactive
region (count:108)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1123 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:35521071-35521413	K562	blood:	n/a	n/a
2	ATF3	chr6:35521065-35521374	K562	blood:	n/a	n/a
3	BACH1	chr6:35536859-35536989	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:35551696-35551950	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr6:35526391-35526712	GM12878	blood:	n/a	n/a
6	BCLAF1	chr6:35551549-35551976	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:35527674-35527807	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:35551643-35551905	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:35527664-35527871	K562	blood:	n/a	n/a
10	BHLHE40	chr6:35526387-35526609	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:35527538-35527879	HepG2	liver:	n/a	n/a
12	BRCA1	chr6:35551734-35551963	HepG2	liver:	n/a	n/a
13	BRCA1	chr6:35551619-35551936	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr6:35520960-35521489	K562	blood:	n/a	n/a
15	CBX3	chr6:35518128-35518651	HCT-116	colon:	n/a	n/a
16	CBX3	chr6:35534503-35534821	K562	blood:	n/a	n/a
17	CBX3	chr6:35564233-35565389	HCT-116	colon:	n/a	n/a
18	CBX3	chr6:35536707-35537063	K562	blood:	n/a	n/a
19	CBX3	chr6:35519985-35520460	K562	blood:	n/a	n/a
20	CBX3	chr6:35534458-35534943	K562	blood:	n/a	n/a
21	CBX3	chr6:35518217-35518567	K562	blood:	n/a	n/a
22	CBX3	chr6:35518192-35518630	K562	blood:	n/a	n/a
23	CBX3	chr6:35564154-35565713	HCT-116	colon:	n/a	n/a
24	CBX3	chr6:35519991-35520537	K562	blood:	n/a	n/a
25	CEBPB	chr6:35551716-35551985	H1-hESC	embryonic stem cell:	n/a	chr6:35551932-35551943
26	CEBPB	chr6:35512717-35512917	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr6:35534664-35534908	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:35564151-35565362	HCT-116	colon:	n/a	n/a
29	CEBPB	chr6:35564079-35565444	HCT-116	colon:	n/a	n/a
30	CEBPB	chr6:35551752-35551992	HepG2	liver:	n/a	chr6:35551932-35551943
31	CEBPB	chr6:35512597-35513014	MCF-7	breast:	n/a	n/a
32	CHD1	chr6:35533324-35533784	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr6:35551676-35552048	GM12878	blood:	n/a	n/a
34	CHD1	chr6:35534176-35534753	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr6:35536884-35537013	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr6:35534696-35534896	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr6:35521009-35521553	K562	blood:	n/a	n/a
38	CREB1	chr6:35521039-35521540	K562	blood:	n/a	n/a
39	CTCF	chr6:35551799-35551825	GM12891	blood:	n/a	n/a
40	CTCF	chr6:35551520-35551790	GM12866	blood:	n/a	n/a
41	CTCF	chr6:35551640-35551790	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr6:35551720-35551870	GM12869	blood:	n/a	n/a
43	CTCF	chr6:35520200-35520350	GM12868	blood:	n/a	n/a
44	CTCF	chr6:35536798-35537060	GM12892	blood:	n/a	chr6:35536914-35536932 chr6:35536917-35536930 chr6:35536798-35536807
45	CTCF	chr6:35551660-35551810	GM12867	blood:	n/a	n/a
46	CTCF	chr6:35536860-35537010	AG09319	gingival:	n/a	chr6:35536914-35536932 chr6:35536917-35536930
47	CTCF	chr6:35551660-35551810	HVMF	connective:	n/a	n/a
48	CTCF	chr6:35520139-35520414	NHEK	skin:	n/a	n/a
49	CTCF	chr6:35551662-35551900	LNCaP	prostate:	n/a	n/a
50	CTCF	chr6:35520200-35520350	NHEK	skin:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35528127-35528177	SAEC	small airway:	n/a
2	chr6:35528127-35528177	SAEC	small airway:	n/a
3	chr6:35565116-35565166	H1-hESC	embryonic stem cell:	embryo
4	chr6:35523658-35523708	HRPEpiC	eye:	n/a
5	chr6:35528127-35528177	SK-N-MC	brain:	n/a
6	chr6:35523658-35523708	HMEC	breast:	n/a
7	chr6:35523700-35523750	NB4	blood:	n/a
8	chr6:35523700-35523750	GM12891	blood:	n/a
9	chr6:35528127-35528177	AG09309	skin:	n/a
10	chr6:35551932-35551982	SK-N-SH_RA	brain:	n/a
11	chr6:35512600-35512650	U87	brain:	n/a
12	chr6:35528127-35528177	GM19239	blood:	n/a
13	chr6:35512600-35512650	AG09309	skin:	n/a
14	chr6:35523700-35523750	HCF	heart:	n/a
15	chr6:35528127-35528177	AG04449	skin:	fetal
16	chr6:35551932-35551982	K562	blood:	n/a
17	chr6:35551932-35551982	T-47D	breast:	n/a
18	chr6:35512600-35512650	SK-N-SH	brain:	n/a
19	chr6:35543610-35543660	MCF10A-Er-Src	breast:	n/a
20	chr6:35551932-35551982	NB4	blood:	n/a
21	chr6:35523700-35523750	MCF10A-Er-Src	breast:	n/a
22	chr6:35528127-35528177	MCF10A-Er-Src	breast:	n/a
23	chr6:35543610-35543660	CMK	blood:	n/a
24	chr6:35523658-35523708	PFSK-1	brain:	n/a
25	chr6:35551932-35551982	HEEpiC	esophagus:	n/a
26	chr6:35523735-35523785	PrEC	prostate:	n/a
27	chr6:35551932-35551982	AG04450	lung:	fetal
28	chr6:35523658-35523708	AG10803	skin:	n/a
29	chr6:35565116-35565166	Jurkat	blood:	n/a
30	chr6:35544468-35544518	NHBE	bronchial:	n/a
31	chr6:35523658-35523708	HEEpiC	esophagus:	n/a
32	chr6:35523658-35523708	GM12891	blood:	n/a
33	chr6:35523735-35523785	HRE	kidney:	n/a
34	chr6:35523658-35523708	HCF	heart:	n/a
35	chr6:35523700-35523750	HAEpiC	amniotic membrane:	n/a
36	chr6:35523735-35523785	SK-N-MC	brain:	n/a
37	chr6:35523735-35523785	PFSK-1	brain:	n/a
38	chr6:35523700-35523750	BJ	skin:	n/a
39	chr6:35523735-35523785	H1-hESC	embryonic stem cell:	embryo
40	chr6:35565116-35565166	MCF10A-Er-Src	breast:	n/a
41	chr6:35523658-35523708	H1-hESC	embryonic stem cell:	embryo
42	chr6:35551932-35551982	ProgFib	skin:	n/a
43	chr6:35523735-35523785	NT2-D1	testis:	n/a
44	chr6:35543610-35543660	LNCaP	prostate:	n/a
45	chr6:35523658-35523708	GM06990	blood:	n/a
46	chr6:35523658-35523708	MCF-7	breast:	n/a
47	chr6:35523735-35523785	NHDF-neo	bronchial:	n/a
48	chr6:35543610-35543660	HepG2	liver:	n/a
49	chr6:35528127-35528177	AoSMC	blood vessel:	n/a
50	chr6:35523700-35523750	HNPCEpiC	eye:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:35525249..35527797-chr6:35704384..35706200,2	MCF-7	breast:
2	chr6:35553086..35555479-chr6:35655198..35657034,2	MCF-7	breast:
3	chr6:35501014..35503138-chr6:35532194..35534250,2	K562	blood:
4	chr6:35550214..35554619-chr6:35701768..35705947,7	K562	blood:
5	chr6:35551325..35552296-chr6:35696466..35697031,2	MCF-7	breast:
6	chr6:35551241..35552671-chr6:35704972..35706000,16	K562	blood:
7	chr6:35562676..35564352-chr6:35607692..35610435,2	K562	blood:
8	chr6:35549719..35551472-chr6:35552354..35554696,2	MCF-7	breast:
9	chr6:35561662..35565304-chr6:35696255..35699445,3	K562	blood:
10	chr6:35501864..35503625-chr6:35509174..35512164,2	K562	blood:
11	chr6:35549719..35551472-chr6:35552354..35554696,2	MCF-7	breast:
12	chr6:35559772..35562715-chr6:35563847..35566628,3	K562	blood:
13	chr6:35536071..35538338-chr6:35539087..35542599,4	K562	blood:
14	chr6:35502232..35503734-chr6:35505671..35507994,2	K562	blood:
15	chr6:35541842..35544127-chr6:35545380..35547353,2	K562	blood:
16	chr6:35436061..35438654-chr6:35541644..35543807,2	K562	blood:
17	chr17:57921307..57924018-chr6:35566994..35568536,2	MCF-7	breast:
18	chr6:35511057..35513907-chr6:35704750..35707121,2	K562	blood:
19	chr6:35551221..35552108-chr6:35591843..35592756,2	MCF-7	breast:
20	chr6:35551273..35551939-chr6:35651991..35652957,3	MCF-7	breast:
21	chr6:35490502..35491010-chr6:35519931..35520659,2	K562	blood:
22	chr6:35564276..35565997-chr6:35567440..35569324,2	MCF-7	breast:
23	chr6:35531994..35534711-chr6:35560308..35562824,2	K562	blood:
24	chr6:35538275..35541551-chr6:35544880..35547832,5	K562	blood:
25	chr6:35557052..35561189-chr6:35693905..35697602,4	K562	blood:
26	chr6:35514449..35517152-chr6:35520311..35522822,2	MCF-7	breast:
27	chr6:35560305..35561817-chr6:35562923..35565288,2	K562	blood:
28	chr6:35531994..35534711-chr6:35560308..35562824,2	K562	blood:
29	chr6:35507228..35509261-chr6:35511378..35514318,2	MCF-7	breast:
30	chr6:35490356..35491291-chr6:35519797..35520709,4	MCF-7	breast:
31	chr6:35548128..35549662-chr6:35699570..35701770,2	K562	blood:
32	chr6:35501014..35503138-chr6:35532194..35534250,2	K562	blood:
33	chr6:35547345..35549326-chr6:35549483..35552184,3	K562	blood:
34	chr6:35557946..35559876-chr6:35570097..35572138,2	K562	blood:
35	chr6:35507266..35509878-chr6:35534285..35536876,2	K562	blood:
36	chr6:35490359..35491197-chr6:35519826..35520699,4	MCF-7	breast:
37	chr6:35549292..35552152-chr6:35564956..35567156,2	MCF-7	breast:
38	chr6:35519589..35521210-chr6:35531779..35534325,2	K562	blood:
39	chr6:35566723..35569701-chr6:35703866..35705522,2	K562	blood:
40	chr6:35501734..35503612-chr6:35506709..35508923,2	K562	blood:
41	chr6:35537206..35539251-chr6:35700274..35702012,2	K562	blood:
42	chr6:35536784..35537384-chr6:35704049..35704824,2	K562	blood:
43	chr6:35552807..35554347-chr6:35560592..35562141,2	K562	blood:
44	chr6:35547345..35549326-chr6:35549483..35552184,3	K562	blood:
45	chr6:35501864..35503625-chr6:35509174..35512164,2	K562	blood:
46	chr6:35567248..35569815-chr6:35570869..35573754,2	MCF-7	breast:
47	chr6:35535434..35538308-chr6:35704866..35707033,2	K562	blood:
48	chr6:35560305..35561817-chr6:35562923..35565288,2	K562	blood:
49	chr6:35556174..35558038-chr6:35568074..35570018,2	MCF-7	breast:
50	chr6:35505532..35508025-chr6:35511062..35512724,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPL10A-1	chr6:35512409-35512482	ENSG00000228559
2	lnc-RPL10A-1	chr6:35512645-35512710	ENSG00000228559
3	lnc-RPL10A-1	chr6:35512992-35513446	ENSG00000228559

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FKBP5	hsa-miR-21-5p	chr6:35542501-35542522
2	FKBP5	hsa-miR-21-5p	chr6:35543161-35543182

Variant related genes	Relation type
ENSG00000228559	TF binding region
ENSG00000219023	TF binding region
ENSG00000228559	CpG island
ENSG00000219023	CpG island
ENSG00000198755	chromatin interactions
ENSG00000007866	chromatin interactions
ENSG00000096060	chromatin interactions
ENSG00000232909	chromatin interactions
ENSG00000228559	chromatin interactions
ENSG00000157343	chromatin interactions
ENSG00000219023	chromatin interactions

Extended variants
information (count: 2644 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2644 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79824616	chr6:35502618-35502619	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs545648737	chr6:35502629-35502630	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs78961571	chr6:35502697-35502698	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs10947554	chr6:35502767-35502768	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs542702128	chr6:35502799-35502800	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs561038200	chr6:35502817-35502818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531726727	chr6:35502863-35502864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548968356	chr6:35502864-35502865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371420383	chr6:35502871-35502872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370843587	chr6:35502895-35502896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs4713883	chr6:35502915-35502916	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs146379657	chr6:35502934-35502935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532193242	chr6:35502962-35502963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368820880	chr6:35502966-35502967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547632159	chr6:35502973-35502974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113323281	chr6:35503033-35503034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112959104	chr6:35503034-35503035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113789983	chr6:35503036-35503037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530022567	chr6:35503053-35503054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536232605	chr6:35503096-35503097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547908691	chr6:35503106-35503107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569744162	chr6:35503119-35503120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537114054	chr6:35503174-35503175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148561827	chr6:35503194-35503195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548739400	chr6:35503203-35503204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532538365	chr6:35503214-35503215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538869281	chr6:35503282-35503283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554437823	chr6:35503321-35503322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562262388	chr6:35503323-35503324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181639321	chr6:35503340-35503341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186848311	chr6:35503345-35503346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191487679	chr6:35503372-35503373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184177036	chr6:35503415-35503416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543481101	chr6:35503416-35503417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2103681	chr6:35503463-35503464	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs571100239	chr6:35503464-35503465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532328572	chr6:35503474-35503475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs3997734	chr6:35503475-35503476	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs559578703	chr6:35503480-35503481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78445475	chr6:35503484-35503485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188734318	chr6:35503485-35503486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77051594	chr6:35503494-35503495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374866383	chr6:35503527-35503528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142904208	chr6:35503529-35503530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552262490	chr6:35503535-35503536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113569474	chr6:35503542-35503543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115659016	chr6:35503545-35503546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7743152	chr6:35503576-35503577	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs150751776	chr6:35503582-35503583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566346747	chr6:35503593-35503594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	19153074	CNVD

Chromatin state (count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35501200-35504600	Enhancers	Fetal Thymus	thymus
2	chr6:35501400-35502800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:35501400-35503400	Enhancers	Fetal Brain Male	brain
4	chr6:35501400-35503600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:35501600-35502800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr6:35501600-35502800	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr6:35501600-35502800	Enhancers	Fetal Muscle Leg	muscle
8	chr6:35501600-35503200	Enhancers	Fetal Stomach	stomach
9	chr6:35501600-35503600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:35501800-35502800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr6:35501800-35503000	Enhancers	Fetal Muscle Trunk	muscle
12	chr6:35501800-35503400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr6:35501800-35503400	Enhancers	Dnd41	blood
14	chr6:35501800-35503600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:35502000-35502800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:35502000-35503200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:35502000-35503200	Enhancers	Placenta	Placenta
18	chr6:35502000-35503800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:35502200-35502800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr6:35502600-35502800	Flanking Active TSS	Thymus	Thymus
21	chr6:35502600-35503000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr6:35502600-35503200	Enhancers	Fetal Brain Female	brain
23	chr6:35502600-35503400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr6:35502600-35503400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:35502600-35503600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr6:35502800-35504000	Enhancers	Thymus	Thymus
27	chr6:35503000-35503200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr6:35503000-35504200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr6:35503200-35504000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr6:35503400-35503600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr6:35503400-35503600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:35503400-35503800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr6:35503400-35504400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr6:35503600-35511200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr6:35503800-35504400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr6:35504000-35504200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:35504200-35505000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr6:35505400-35505600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr6:35506800-35507000	Enhancers	Fetal Muscle Trunk	muscle
40	chr6:35509600-35510200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr6:35509600-35510400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr6:35509800-35510000	Enhancers	Placenta Amnion	Placenta Amnion
43	chr6:35509800-35510200	Enhancers	Primary hematopoietic stem cells	blood
44	chr6:35510000-35510200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:35510000-35510200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:35510000-35512400	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr6:35510200-35511200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr6:35510200-35512400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:35510400-35511400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr6:35511000-35511400	Enhancers	H9 Cell Line	embryonic stem cell

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