Variant report

Variant	nsv602833
Chromosome Location	chr6:33534880-33588147
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3404)
CpG islands
(count:2385)
Chromatin interactive
region (count:134)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:3404 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:33551450-33551638	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:33557623-33558302	K562	blood:	n/a	n/a
3	ARID3A	chr6:33557460-33558338	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:33558643-33558885	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:33553467-33553714	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:33547880-33548462	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:33581113-33581503	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:33547967-33548208	K562	blood:	n/a	n/a
9	ATF1	chr6:33547888-33548200	K562	blood:	n/a	n/a
10	ATF2	chr6:33546555-33546874	GM12878	blood:	n/a	n/a
11	ATF2	chr6:33553354-33553783	GM12878	blood:	n/a	n/a
12	ATF2	chr6:33560263-33560584	GM12878	blood:	n/a	n/a
13	ATF2	chr6:33564809-33565065	GM12878	blood:	n/a	n/a
14	ATF2	chr6:33538865-33539411	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr6:33538206-33539508	GM12878	blood:	n/a	n/a
16	ATF2	chr6:33538263-33539510	GM12878	blood:	n/a	n/a
17	ATF2	chr6:33560114-33560756	GM12878	blood:	n/a	n/a
18	ATF3	chr6:33553301-33553953	GM12878	blood:	n/a	n/a
19	ATF3	chr6:33557982-33558308	HepG2	liver:	n/a	n/a
20	ATF3	chr6:33558058-33558269	K562	blood:	n/a	n/a
21	ATF3	chr6:33557963-33558360	K562	blood:	n/a	n/a
22	ATF3	chr6:33553403-33553709	K562	blood:	n/a	n/a
23	BACH1	chr6:33538874-33539043	K562	blood:	n/a	n/a
24	BACH1	chr6:33539573-33539580	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr6:33553463-33553777	K562	blood:	n/a	n/a
26	BACH1	chr6:33576845-33577141	K562	blood:	n/a	n/a
27	BACH1	chr6:33560763-33561165	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr6:33574858-33575263	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:33553357-33553800	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:33547955-33548135	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr6:33538446-33539235	GM12878	blood:	n/a	n/a
32	BATF	chr6:33538460-33539009	GM12878	blood:	n/a	n/a
33	BATF	chr6:33558012-33558303	GM12878	blood:	n/a	chr6:33558096-33558106 chr6:33558177-33558188
34	BCL11A	chr6:33538517-33539015	GM12878	blood:	n/a	n/a
35	BCL11A	chr6:33558049-33558273	GM12878	blood:	n/a	n/a
36	BCL11A	chr6:33538446-33539220	GM12878	blood:	n/a	chr6:33539194-33539203
37	BCL3	chr6:33538484-33539425	GM12878	blood:	n/a	chr6:33539194-33539203
38	BCL3	chr6:33538743-33539226	A549	lung:	n/a	chr6:33539194-33539203
39	BCL3	chr6:33538774-33539305	A549	lung:	n/a	chr6:33539194-33539203
40	BCLAF1	chr6:33538319-33539469	GM12878	blood:	n/a	chr6:33539194-33539203
41	BCLAF1	chr6:33560764-33561395	GM12878	blood:	n/a	chr6:33561177-33561186
42	BCLAF1	chr6:33553359-33553838	GM12878	blood:	n/a	n/a
43	BCLAF1	chr6:33538473-33539466	GM12878	blood:	n/a	chr6:33539194-33539203
44	BCLAF1	chr6:33560131-33560550	GM12878	blood:	n/a	n/a
45	BCLAF1	chr6:33547755-33548301	GM12878	blood:	n/a	chr6:33548004-33548017
46	BHLHE40	chr6:33553407-33553754	HepG2	liver:	n/a	n/a
47	BHLHE40	chr6:33553351-33553770	K562	blood:	n/a	n/a
48	BHLHE40	chr6:33557469-33558785	HepG2	liver:	n/a	n/a
49	BHLHE40	chr6:33581084-33581617	HepG2	liver:	n/a	n/a
50	BHLHE40	chr6:33575607-33575970	HepG2	liver:	n/a	n/a

(count:2385 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33561264-33561314	CMK	blood:	n/a
2	chr6:33561099-33561149	PFSK-1	brain:	n/a
3	chr6:33561181-33561231	Caco-2	colon:	n/a
4	chr6:33561266-33561316	AG04450	lung:	fetal
5	chr6:33547978-33548028	MCF10A-Er-Src	breast:	n/a
6	chr6:33539085-33539135	GM06990	blood:	n/a
7	chr6:33561264-33561314	CMK	blood:	n/a
8	chr6:33561099-33561149	PFSK-1	brain:	n/a
9	chr6:33561181-33561231	Caco-2	colon:	n/a
10	chr6:33561266-33561316	AG04450	lung:	fetal
11	chr6:33547978-33548028	MCF10A-Er-Src	breast:	n/a
12	chr6:33539085-33539135	GM06990	blood:	n/a
13	chr6:33548425-33548475	HNPCEpiC	eye:	n/a
14	chr6:33550038-33550088	AG04449	skin:	fetal
15	chr6:33548127-33548177	HepG2	liver:	n/a
16	chr6:33561449-33561499	IMR90	lung:	fetal
17	chr6:33561264-33561314	AG04450	lung:	fetal
18	chr6:33539085-33539135	NHBE	bronchial:	n/a
19	chr6:33587496-33587546	HIPEpiC	eye:	n/a
20	chr6:33561186-33561236	NH-A	brain:	n/a
21	chr6:33547978-33548028	Hela-S3	cervix:	n/a
22	chr6:33561253-33561303	HIPEpiC	eye:	n/a
23	chr6:33547980-33548030	SAEC	small airway:	n/a
24	chr6:33539085-33539135	HAEpiC	amniotic membrane:	n/a
25	chr6:33558433-33558483	HUVEC	blood vessel:	n/a
26	chr6:33538714-33538764	GM06990	blood:	n/a
27	chr6:33561253-33561303	HRPEpiC	eye:	n/a
28	chr6:33561253-33561303	HMEC	breast:	n/a
29	chr6:33548425-33548475	MCF10A-Er-Src	breast:	n/a
30	chr6:33562509-33562559	PrEC	prostate:	n/a
31	chr6:33585071-33585121	GM12878	blood:	n/a
32	chr6:33539338-33539388	HEK293	kidney:	embryo
33	chr6:33561186-33561236	GM12878	blood:	n/a
34	chr6:33538979-33539029	PrEC	prostate:	n/a
35	chr6:33547969-33548019	NT2-D1	testis:	n/a
36	chr6:33548425-33548475	CMK	blood:	n/a
37	chr6:33548009-33548059	HepG2	liver:	n/a
38	chr6:33547978-33548028	HRPEpiC	eye:	n/a
39	chr6:33548423-33548473	ECC-1	luminal epithelium:	n/a
40	chr6:33549186-33549236	AG04449	skin:	fetal
41	chr6:33563311-33563361	AG09319	gingival:	n/a
42	chr6:33548423-33548473	AG09309	skin:	n/a
43	chr6:33541445-33541495	HAEpiC	amniotic membrane:	n/a
44	chr6:33561188-33561238	GM06990	blood:	n/a
45	chr6:33551533-33551583	Hepatocyte	liver:	n/a
46	chr6:33536144-33536194	SKMC	muscle:	n/a
47	chr6:33539085-33539135	NT2-D1	testis:	n/a
48	chr6:33550038-33550088	GM06990	blood:	n/a
49	chr6:33561266-33561316	Hepatocyte	liver:	n/a
50	chr6:33561449-33561499	HIPEpiC	eye:	n/a

(count:134 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:33567428..33569467-chr6:33588119..33589840,2	MCF-7	breast:
2	chr6:33381203..33384118-chr6:33546265..33549089,2	K562	blood:
3	chr6:33576269..33579262-chr6:33600060..33601906,2	MCF-7	breast:
4	chr6:33382621..33385389-chr6:33558718..33560996,2	K562	blood:
5	chr6:33569313..33571736-chr6:33599981..33602556,2	K562	blood:
6	chr6:33556929..33558055-chr6:33575240..33576451,8	MCF-7	breast:
7	chr6:33557569..33559223-chr6:33672789..33674425,2	K562	blood:
8	chr6:33557542..33558049-chr6:33667963..33668918,2	MCF-7	breast:
9	chr6:33537267..33540253-chr6:33551095..33553614,3	K562	blood:
10	chr6:33536613..33539410-chr6:33637420..33640374,2	K562	blood:
11	chr6:33546298..33549471-chr6:33550091..33553469,5	K562	blood:
12	chr6:33577318..33579921-chr6:33582665..33584246,2	K562	blood:
13	chr6:33547287..33549306-chr6:33551969..33553577,2	K562	blood:
14	chr6:33574216..33577618-chr6:33579266..33582393,4	MCF-7	breast:
15	chr6:33587172..33590152-chr6:34203876..34205466,2	K562	blood:
16	chr6:33379174..33381010-chr6:33538458..33541414,2	K562	blood:
17	chr6:33517814..33520773-chr6:33534546..33536789,2	K562	blood:
18	chr6:33384739..33386700-chr6:33551719..33554109,2	MCF-7	breast:
19	chr6:33562478..33565325-chr6:33572841..33575005,2	MCF-7	breast:
20	chr6:33587667..33592228-chr6:33677016..33679936,5	MCF-7	breast:
21	chr6:33551901..33555908-chr6:33676752..33679381,5	K562	blood:
22	chr6:33533712..33536819-chr6:33537641..33540205,3	MCF-7	breast:
23	chr6:33553164..33555974-chr6:33639876..33642136,2	MCF-7	breast:
24	chr6:33557167..33558102-chr6:33640434..33641022,2	MCF-7	breast:
25	chr6:33532988..33536659-chr6:33537187..33540995,4	K562	blood:
26	chr6:33557128..33558070-chr6:33729670..33730677,6	K562	blood:
27	chr6:33556084..33559190-chr6:33561463..33564085,3	K562	blood:
28	chr6:33541749..33544429-chr6:33546198..33547784,2	MCF-7	breast:
29	chr6:33375962..33378534-chr6:33537596..33540481,2	K562	blood:
30	chr18:18691523..18692461-chr6:33588062..33589054,2	Hela-S3	cervix:
31	chr6:33554633..33558061-chr6:33675915..33678804,3	MCF-7	breast:
32	chr6:33562478..33565325-chr6:33572841..33575005,2	MCF-7	breast:
33	chr6:33533870..33536735-chr6:33537311..33539466,2	MCF-7	breast:
34	chr6:33538816..33540942-chr6:33543611..33545834,3	MCF-7	breast:
35	chr6:33556983..33559426-chr6:33569915..33571800,2	MCF-7	breast:
36	chr6:33557322..33558111-chr6:33667371..33668903,6	MCF-7	breast:
37	chr6:33567572..33569907-chr6:33573549..33575919,2	MCF-7	breast:
38	chr6:33545816..33547496-chr6:33675270..33677360,2	K562	blood:
39	chr6:33538758..33539282-chr6:33548033..33548541,2	K562	blood:
40	chr6:33561930..33564001-chr6:33577360..33579939,2	K562	blood:
41	chr19:50432772..50433317-chr6:33548039..33548579,2	NB4	blood:
42	chr6:33420326..33423381-chr6:33545501..33547721,3	MCF-7	breast:
43	chr6:33556676..33558804-chr6:33667221..33669587,2	K562	blood:
44	chr6:33557862..33560664-chr6:33667390..33670226,3	MCF-7	breast:
45	chr6:33557935..33558471-chr6:33567388..33568017,2	MCF-7	breast:
46	chr6:33538758..33539282-chr6:33548033..33548541,2	K562	blood:
47	chr6:33553147..33553827-chr6:33730088..33730602,2	K562	blood:
48	chr6:33537234..33540947-chr6:33547325..33549534,4	K562	blood:
49	chr6:33538231..33539799-chr6:33543255..33545002,2	K562	blood:
50	chr6:33557311..33558097-chr6:33600135..33601024,5	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAK1-1	chr6:33553883-33555647	ENSG00000197251.3
2	lnc-GGNBP1-1	chr6:33552505-33552617	NR_028361
3	lnc-BAK1-1	chr6:33560774-33561115	ENSG00000197251.3
4	lnc-GGNBP1-1	chr6:33554447-33554565	NR_028361
5	lnc-GGNBP1-1	chr6:33552996-33553144	NR_028361
6	lnc-GGNBP1-1	chr6:33556690-33556803	NR_028361
7	lnc-GGNBP1-1	chr6:33553367-33553498	NR_028361
8	lnc-GGNBP1-1	chr6:33551476-33551847	NR_028361

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	BAK1	hsa-miR-92a-3p	chr6:33540335-33540360
2	BAK1	hsa-miR-125b-5p	chr6:33540949-33540942
3	BAK1	hsa-miR-125b-5p	chr6:33540943-33540964
4	BAK1	hsa-miR-125a-5p	chr6:33540949-33540942
5	BAK1	hsa-miR-125a-5p	chr6:33540943-33540963

Variant related genes	Relation type
LINC00336	TF binding region
GGNBP1	TF binding region
ITPR3	TF binding region
BAK1	TF binding region
LINC00336	CpG island
GGNBP1	CpG island
ITPR3	CpG island
BAK1	CpG island
ENSG00000161904	chromatin interactions
ENSG00000231500	chromatin interactions
ENSG00000112514	chromatin interactions
ENSG00000096433	chromatin interactions
ENSG00000197251	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000197283	chromatin interactions
ENSG00000163872	chromatin interactions
ENSG00000112511	chromatin interactions
ENSG00000213024	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000030110	chromatin interactions
ENSG00000225644	chromatin interactions
ENSG00000104951	chromatin interactions
ENSG00000137288	chromatin interactions
ENSG00000204188	chromatin interactions
ENSG00000237649	chromatin interactions
ENSG00000196584	chromatin interactions
ENSG00000067900	chromatin interactions
ENSG00000213588	chromatin interactions

Extended variants
information (count: 2227 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:2227 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6914422	chr6:33534880-33534881	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373261112	chr6:33534891-33534892	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548252998	chr6:33534919-33534920	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569578834	chr6:33534954-33534955	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146432372	chr6:33534965-33534966	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558862457	chr6:33535041-33535042	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs183985288	chr6:33535087-33535088	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs534937964	chr6:33535107-33535108	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs187118047	chr6:33535169-33535170	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs574939896	chr6:33535173-33535174	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs541991442	chr6:33535189-33535190	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs373510637	chr6:33535195-33535196	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs563777740	chr6:33535269-33535270	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376919638	chr6:33535318-33535319	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575594378	chr6:33535325-33535326	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536339235	chr6:33535363-33535364	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546231391	chr6:33535383-33535384	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564429937	chr6:33535440-33535441	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs210131	chr6:33535466-33535467	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs139049502	chr6:33535528-33535529	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113245543	chr6:33535598-33535599	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563396598	chr6:33535604-33535605	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530480177	chr6:33535648-33535649	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545409809	chr6:33535651-33535652	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35512263	chr6:33535687-33535688	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559319727	chr6:33535696-33535697	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373234924	chr6:33535704-33535705	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563709848	chr6:33535706-33535707	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192035648	chr6:33535723-33535724	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569722584	chr6:33535733-33535734	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62407565	chr6:33535739-33535740	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs551757729	chr6:33535749-33535750	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62407566	chr6:33535786-33535787	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs534998775	chr6:33535835-33535836	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559787583	chr6:33535838-33535839	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs76299936	chr6:33535941-33535942	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs78581891	chr6:33535966-33535967	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376644541	chr6:33535977-33535978	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34521623	chr6:33535979-33535980	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184223130	chr6:33535991-33535992	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74610062	chr6:33536004-33536005	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111281508	chr6:33536007-33536008	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190080531	chr6:33536030-33536031	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182209313	chr6:33536044-33536045	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185593604	chr6:33536061-33536062	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573259336	chr6:33536066-33536067	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376508347	chr6:33536081-33536082	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537511570	chr6:33536082-33536083	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541365219	chr6:33536140-33536141	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189442123	chr6:33536141-33536142	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
abnormal development	18461090	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
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:3107 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33516800-33537600	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr6:33530400-33536800	Weak transcription	K562	blood
3	chr6:33530400-33537600	Weak transcription	GM12878-XiMat	blood
4	chr6:33530400-33538800	Weak transcription	Esophagus	oesophagus
5	chr6:33531000-33538200	Weak transcription	Primary T cells from cord blood	blood
6	chr6:33531400-33538400	Weak transcription	Osteobl	bone
7	chr6:33533200-33538400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr6:33533200-33538600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:33533600-33535800	Weak transcription	Fetal Stomach	stomach
10	chr6:33533600-33537600	Weak transcription	Fetal Thymus	thymus
11	chr6:33533800-33535400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:33533800-33536000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr6:33533800-33538400	Weak transcription	Rectal Smooth Muscle	rectum
14	chr6:33534000-33535000	Enhancers	NHEK	skin
15	chr6:33534200-33535000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:33534200-33535000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:33534200-33538600	Weak transcription	Fetal Muscle Leg	muscle
18	chr6:33534400-33535000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:33534400-33535000	Enhancers	HMEC	breast
20	chr6:33534400-33535200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:33534400-33536000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr6:33534400-33538400	Weak transcription	Duodenum Mucosa	Duodenum
23	chr6:33534600-33535000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr6:33534600-33536000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr6:33534600-33536000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr6:33534600-33536000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr6:33534600-33538400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr6:33534600-33538600	Weak transcription	Fetal Intestine Small	intestine
29	chr6:33534600-33538800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr6:33534800-33536000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr6:33534800-33537800	Weak transcription	Thymus	Thymus
32	chr6:33534800-33538400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr6:33534800-33538400	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr6:33535000-33535200	Flanking Active TSS	NHEK	skin
35	chr6:33535000-33536200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr6:33535000-33538200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr6:33535000-33538400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr6:33535000-33538600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr6:33535000-33538600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr6:33535000-33538600	Weak transcription	HMEC	breast
41	chr6:33535200-33535600	Enhancers	NHEK	skin
42	chr6:33535200-33536000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr6:33535200-33538400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr6:33535200-33538400	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr6:33535400-33536000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr6:33535400-33538400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:33535600-33536200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr6:33535600-33536200	Enhancers	Brain Germinal Matrix	brain
49	chr6:33535600-33538400	Weak transcription	NHEK	skin
50	chr6:33535600-33538400	Weak transcription	NHLF	lung

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