Variant report

Variant	esv2756864
Chromosome Location	chr1:151328794-151411635
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1634)
CpG islands
(count:1649)
Chromatin interactive
region (count:231)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:11)

(count:1634 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:151371751-151372339	K562	blood:	n/a	chr1:151372120-151372135
2	ARID3A	chr1:151345015-151345215	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:151371733-151372165	HepG2	liver:	n/a	chr1:151372120-151372135
4	ATF1	chr1:151357084-151357455	K562	blood:	n/a	n/a
5	ATF1	chr1:151371742-151372196	K562	blood:	n/a	n/a
6	ATF2	chr1:151371724-151372171	GM12878	blood:	n/a	n/a
7	ATF2	chr1:151371634-151372180	GM12878	blood:	n/a	n/a
8	ATF2	chr1:151371626-151372256	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr1:151371732-151372222	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr1:151371725-151372346	A549	lung:	n/a	n/a
11	ATF3	chr1:151368851-151369032	K562	blood:	n/a	n/a
12	BACH1	chr1:151371808-151372310	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:151405549-151405676	K562	blood:	n/a	n/a
14	BACH1	chr1:151405126-151405250	K562	blood:	n/a	n/a
15	BCL3	chr1:151371666-151372235	A549	lung:	n/a	chr1:151372009-151372018
16	BCL3	chr1:151375014-151375704	A549	lung:	n/a	n/a
17	BCL3	chr1:151371693-151373473	A549	lung:	n/a	chr1:151372009-151372018
18	BCL3	chr1:151373524-151374156	A549	lung:	n/a	n/a
19	BCL3	chr1:151372480-151372962	GM12878	blood:	n/a	n/a
20	BCL3	chr1:151345733-151346070	GM12878	blood:	n/a	n/a
21	BCLAF1	chr1:151371705-151372350	GM12878	blood:	n/a	chr1:151372009-151372018
22	BCLAF1	chr1:151371605-151372282	GM12878	blood:	n/a	chr1:151372009-151372018
23	BHLHE40	chr1:151345650-151345906	HepG2	liver:	n/a	n/a
24	BHLHE40	chr1:151344946-151345289	K562	blood:	n/a	n/a
25	BHLHE40	chr1:151342372-151343265	K562	blood:	n/a	n/a
26	BHLHE40	chr1:151356747-151357326	K562	blood:	n/a	n/a
27	BRCA1	chr1:151372596-151372778	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr1:151345169-151345211	HepG2	liver:	n/a	n/a
29	BRCA1	chr1:151371813-151372175	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr1:151360096-151360428	K562	blood:	n/a	n/a
31	CBX3	chr1:151334672-151335188	K562	blood:	n/a	n/a
32	CBX3	chr1:151342983-151343411	K562	blood:	n/a	n/a
33	CBX3	chr1:151358593-151358947	K562	blood:	n/a	n/a
34	CBX3	chr1:151334633-151335302	K562	blood:	n/a	n/a
35	CBX3	chr1:151371662-151372200	K562	blood:	n/a	n/a
36	CCNT2	chr1:151372277-151372477	K562	blood:	n/a	n/a
37	CCNT2	chr1:151343082-151343282	K562	blood:	n/a	n/a
38	CCNT2	chr1:151357075-151357435	K562	blood:	n/a	n/a
39	CEBPB	chr1:151388793-151389072	K562	blood:	n/a	chr1:151388928-151388939
40	CEBPB	chr1:151407815-151407820	K562	blood:	n/a	n/a
41	CEBPB	chr1:151368794-151369106	H1-hESC	embryonic stem cell:	n/a	chr1:151368942-151368953
42	CEBPB	chr1:151343930-151344227	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr1:151371720-151372181	ECC-1	luminal epithelium:	n/a	chr1:151371884-151371895
44	CEBPB	chr1:151371703-151372202	HepG2	liver:	n/a	chr1:151371884-151371895
45	CEBPB	chr1:151392443-151392803	A549	lung:	n/a	chr1:151392614-151392625
46	CEBPB	chr1:151371621-151372822	MCF-7	breast:	n/a	chr1:151371884-151371895
47	CEBPB	chr1:151345110-151345191	HepG2	liver:	n/a	n/a
48	CEBPB	chr1:151388787-151389075	K562	blood:	n/a	chr1:151388928-151388939
49	CEBPB	chr1:151328846-151328978	A549	lung:	n/a	chr1:151328890-151328901
50	CEBPB	chr1:151371730-151372070	HepG2	liver:	n/a	chr1:151371884-151371895

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151372572-151372622	GM12891	blood:	n/a
2	chr1:151371309-151371359	HEEpiC	esophagus:	n/a
3	chr1:151372572-151372622	GM12891	blood:	n/a
4	chr1:151371309-151371359	HEEpiC	esophagus:	n/a
5	chr1:151370645-151370695	NHBE	bronchial:	n/a
6	chr1:151372581-151372631	HMEC	breast:	n/a
7	chr1:151400745-151400795	GM06990	blood:	n/a
8	chr1:151371944-151371994	PrEC	prostate:	n/a
9	chr1:151372335-151372385	ovcar-3	ovarian:	n/a
10	chr1:151399683-151399733	NH-A	brain:	n/a
11	chr1:151372652-151372702	MCF10A-Er-Src	breast:	n/a
12	chr1:151346048-151346098	HEEpiC	esophagus:	n/a
13	chr1:151372335-151372385	GM19239	blood:	n/a
14	chr1:151372581-151372631	AG04450	lung:	fetal
15	chr1:151345181-151345231	HCM	heart:	n/a
16	chr1:151372228-151372278	MCF10A-Er-Src	breast:	n/a
17	chr1:151372228-151372278	CMK	blood:	n/a
18	chr1:151402121-151402171	IMR90	lung:	fetal
19	chr1:151371309-151371359	AG04449	skin:	fetal
20	chr1:151345181-151345231	MCF-7	breast:	n/a
21	chr1:151343840-151343890	IMR90	lung:	fetal
22	chr1:151371972-151372022	SAEC	small airway:	n/a
23	chr1:151336795-151336845	AG04449	skin:	fetal
24	chr1:151371944-151371994	K562	blood:	n/a
25	chr1:151372572-151372622	A549	lung:	n/a
26	chr1:151345123-151345173	PrEC	prostate:	n/a
27	chr1:151336795-151336845	NHBE	bronchial:	n/a
28	chr1:151402121-151402171	GM12891	blood:	n/a
29	chr1:151336795-151336845	BE2_C	brain:	n/a
30	chr1:151372228-151372278	HRE	kidney:	n/a
31	chr1:151345123-151345173	SAEC	small airway:	n/a
32	chr1:151372652-151372702	PANC-1	pancreas:	n/a
33	chr1:151369469-151369519	GM06990	blood:	n/a
34	chr1:151336795-151336845	HMEC	breast:	n/a
35	chr1:151400745-151400795	PrEC	prostate:	n/a
36	chr1:151345181-151345231	AG04450	lung:	fetal
37	chr1:151372147-151372197	AG04449	skin:	fetal
38	chr1:151344806-151344856	GM06990	blood:	n/a
39	chr1:151399683-151399733	SK-N-SH	brain:	n/a
40	chr1:151372581-151372631	ovcar-3	ovarian:	n/a
41	chr1:151346048-151346098	SAEC	small airway:	n/a
42	chr1:151346122-151346172	GM12892	blood:	n/a
43	chr1:151372335-151372385	Hepatocyte	liver:	n/a
44	chr1:151346122-151346172	IMR90	lung:	fetal
45	chr1:151345123-151345173	HMEC	breast:	n/a
46	chr1:151345771-151345821	RPTEC	kidney:	n/a
47	chr1:151346048-151346098	HRCEpiC	kidney:	n/a
48	chr1:151345771-151345821	Hepatocyte	liver:	n/a
49	chr1:151371285-151371335	A549	lung:	n/a
50	chr1:151372147-151372197	A549	lung:	n/a

(count:231 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	1:151180715-151199990..1:151324693-151329948	GM12878	blood:
2	chr1:151389430..151391036-chr1:151431116..151432632,2	MCF-7	breast:
3	chr1:151368568..151371370-chr1:151392039..151394565,2	K562	blood:
4	chr1:151252229..151256416-chr1:151370480..151373573,6	MCF-7	breast:
5	chr1:151373766..151375598-chr1:151437855..151440411,2	K562	blood:
6	1:151329948-151333184..1:151516085-151535167	Hela-S3	cervix:
7	chr1:151387420..151389134-chr1:151433019..151434724,2	K562	blood:
8	chr1:151342418..151344978-chr1:151361696..151364403,2	MCF-7	breast:
9	1:151203965-151215310..1:151402394-151411623	GM12878	blood:
10	1:151324693-151329948..1:151516085-151535167	GM12878	blood:
11	chr1:151379379..151381233-chr1:151511239..151513051,2	MCF-7	breast:
12	chr1:151371526..151374105-chr1:151428160..151432357,4	K562	blood:
13	chr1:151319407..151322212-chr1:151384935..151387557,2	K562	blood:
14	1:151375897-151378579..1:151618750-151636526	Hela-S3	cervix:
15	chr1:151298715..151300740-chr1:151336029..151338584,2	K562	blood:
16	1:151158061-151171193..1:151324693-151329948	GM12878	blood:
17	1:151219411-151234038..1:151329948-151333184	Hela-S3	cervix:
18	chr1:151335152..151338036-chr1:151343299..151345232,3	MCF-7	breast:
19	chr1:151409926..151411809-chr1:151413476..151415968,2	MCF-7	breast:
20	chr1:151162193..151163907-chr1:151370731..151372764,2	MCF-7	breast:
21	chr1:151348976..151351066-chr1:151352472..151354650,2	K562	blood:
22	chr1:151337000..151339561-chr1:151374303..151377046,2	MCF-7	breast:
23	1:151393910-151394636..1:151411623-151426875	Hela-S3	cervix:
24	chr1:151312120..151316742-chr1:151370081..151375586,6	MCF-7	breast:
25	chr1:151343373..151350462-chr1:151369795..151376328,11	MCF-7	breast:
26	chr1:151353527..151355666-chr1:151374191..151375959,2	K562	blood:
27	chr1:151336320..151338868-chr1:151344785..151346534,2	K562	blood:
28	chr1:151316826..151319751-chr1:151342092..151344070,3	MCF-7	breast:
29	chr1:151268846..151270969-chr1:151374087..151376100,2	MCF-7	breast:
30	chr1:151317602..151320403-chr1:151337333..151341038,5	MCF-7	breast:
31	chr1:151335378..151338148-chr1:151374572..151377494,3	MCF-7	breast:
32	chr1:151265701..151267692-chr1:151376105..151378029,2	MCF-7	breast:
33	chr1:151341989..151348019-chr1:151370228..151376359,14	MCF-7	breast:
34	chr1:151351127..151353952-chr1:151357831..151359391,2	K562	blood:
35	chr1:151363150..151367072-chr1:151371054..151375745,5	MCF-7	breast:
36	chr1:151341989..151348019-chr1:151370228..151376359,14	MCF-7	breast:
37	chr1:151297425..151301136-chr1:151370895..151373723,5	MCF-7	breast:
38	chr1:151041688..151044395-chr1:151373966..151376267,2	K562	blood:
39	1:151324693-151329948..1:151496437-151509688	Hela-S3	cervix:
40	chr1:151319574..151321193-chr1:151343801..151346115,3	MCF-7	breast:
41	chr1:151335378..151338148-chr1:151374572..151377494,3	MCF-7	breast:
42	chr1:151377630..151380310-chr1:151382827..151386169,3	K562	blood:
43	chr1:151337330..151339100-chr1:151341997..151344198,2	K562	blood:
44	1:151353564-151358657..1:151411623-151426875	Hela-S3	cervix:
45	1:151246650-151254384..1:151375897-151378579	Hela-S3	cervix:
46	chr1:151312109..151317002-chr1:151372398..151376596,7	MCF-7	breast:
47	chr1:151253607..151256454-chr1:151374853..151377670,2	MCF-7	breast:
48	chr1:151373885..151375953-chr1:151382352..151386017,5	K562	blood:
49	chr1:151317696..151319917-chr1:151365664..151368589,2	MCF-7	breast:
50	1:151270864-151283078..1:151358657-151368243	K562	blood:

No data

(count:11 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	POGZ	hsa-miR-17-5p	chr1:151376717-151376739
2	POGZ	hsa-miR-9-5p	chr1:151377089-151377112
3	POGZ	hsa-miR-19b-3p	chr1:151376496-151376518
4	POGZ	hsa-miR-221-3p	chr1:151376785-151376779
5	POGZ	hsa-miR-221-3p	chr1:151376779-151376802
6	POGZ	hsa-miR-20a-5p	chr1:151376717-151376739
7	SELENBP1	hsa-miR-335-5p	chr1:151336816-151336837
8	POGZ	hsa-miR-34a-5p	chr1:151376085-151376106
9	POGZ	hsa-miR-130b-3p	chr1:151376495-151376516
10	POGZ	hsa-miR-34a-5p	chr1:151376091-151376084
11	SELENBP1	hsa-miR-92a-3p	chr1:151336887-151336908

Variant related genes	Relation type
SELENBP1	TF binding region
POGZ	TF binding region
PSMB4	TF binding region
RNY4P25	TF binding region
SELENBP1	CpG island
POGZ	CpG island
PSMB4	CpG island
RNY4P25	CpG island
ENSG00000119878	chromatin interactions
ENSG00000143393	chromatin interactions
ENSG00000238711	chromatin interactions
ENSG00000151665	chromatin interactions
ENSG00000143375	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000143442	chromatin interactions
ENSG00000163141	chromatin interactions
ENSG00000143416	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000225556	chromatin interactions
ENSG00000143390	chromatin interactions
ENSG00000143398	chromatin interactions
ENSG00000143450	chromatin interactions
ENSG00000252840	chromatin interactions
ENSG00000159377	chromatin interactions
ENSG00000265753	chromatin interactions
ENSG00000224645	chromatin interactions
ENSG00000143458	chromatin interactions
ENSG00000237976	chromatin interactions
ENSG00000273481	chromatin interactions
ENSG00000206635	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000143376	chromatin interactions
ENSG00000159352	chromatin interactions
ENSG00000197622	chromatin interactions
ENSG00000163159	chromatin interactions
ENSG00000223861	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000143436	chromatin interactions
ENSG00000207606	chromatin interactions

Extended variants
information (count: 3262 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:3262 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs744536	chr1:151328794-151328795	Weak transcription	Chromatin interactive region	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572614077	chr1:151328824-151328825	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
3	rs573207027	chr1:151328840-151328841	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
4	rs541722955	chr1:151328866-151328867	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
5	rs148365644	chr1:151328982-151328983	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
6	rs561294156	chr1:151329009-151329010	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
7	rs141569775	chr1:151329023-151329024	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
8	rs543526291	chr1:151329037-151329038	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
9	rs150890129	chr1:151329061-151329062	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
10	rs138259362	chr1:151329083-151329084	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
11	rs368998292	chr1:151329114-151329115	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
12	rs2769272	chr1:151329138-151329139	Weak transcription	Chromatin interactive region	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs528348182	chr1:151329149-151329150	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
14	rs377178401	chr1:151329159-151329160	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
15	rs548493079	chr1:151329264-151329265	Weak transcription Enhancers	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
16	rs565250420	chr1:151329347-151329348	Weak transcription Enhancers	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
17	rs149597613	chr1:151329400-151329401	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
18	rs118041983	chr1:151329407-151329408	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
19	rs549861955	chr1:151329523-151329524	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
20	rs569770462	chr1:151329533-151329534	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
21	rs183013225	chr1:151329549-151329550	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
22	rs369990280	chr1:151329594-151329595	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
23	rs147262987	chr1:151329603-151329604	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
24	rs577324882	chr1:151329617-151329618	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
25	rs140737042	chr1:151329620-151329621	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
26	rs75421372	chr1:151329651-151329652	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
27	rs35563802	chr1:151329679-151329680	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
28	rs555334711	chr1:151329690-151329691	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
29	rs558643955	chr1:151329697-151329698	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
30	rs186961549	chr1:151329755-151329756	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
31	rs144572922	chr1:151329766-151329767	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
32	rs75000508	chr1:151329781-151329782	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
33	rs200563197	chr1:151329782-151329783	Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
34	rs191544452	chr1:151329805-151329806	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
35	rs75236137	chr1:151329843-151329844	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
36	rs528123693	chr1:151329910-151329911	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
37	rs548180601	chr1:151329925-151329926	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
38	rs182464094	chr1:151329938-151329939	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
39	rs147221741	chr1:151330017-151330018	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs368275253	chr1:151330044-151330045	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs550323371	chr1:151330049-151330050	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs148701946	chr1:151330064-151330065	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs187935574	chr1:151330073-151330074	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs570158419	chr1:151330079-151330080	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs552665004	chr1:151330098-151330099	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs193022897	chr1:151330161-151330162	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs142219770	chr1:151330187-151330188	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs111586482	chr1:151330212-151330213	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs2800951	chr1:151330289-151330290	Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs575139403	chr1:151330303-151330304	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21138945	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2231 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151328400-151334600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr1:151328400-151336000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:151328600-151329200	Weak transcription	K562	blood
4	chr1:151328600-151334800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr1:151329200-151329400	Enhancers	Osteobl	bone
6	chr1:151329200-151329800	Enhancers	K562	blood
7	chr1:151329400-151329600	Enhancers	Colonic Mucosa	Colon
8	chr1:151329400-151329800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr1:151329400-151340600	Weak transcription	Osteobl	bone
10	chr1:151329600-151336600	Weak transcription	Rectal Smooth Muscle	rectum
11	chr1:151329600-151336800	Weak transcription	Colonic Mucosa	Colon
12	chr1:151329800-151334400	Weak transcription	K562	blood
13	chr1:151329800-151334600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:151331400-151334600	Weak transcription	Lung	lung
15	chr1:151331600-151334600	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr1:151331600-151334800	Weak transcription	Right Ventricle	heart
17	chr1:151332200-151334600	Weak transcription	Fetal Intestine Small	intestine
18	chr1:151332200-151334800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr1:151332200-151340000	Weak transcription	Fetal Heart	heart
20	chr1:151332600-151334400	Weak transcription	Fetal Lung	lung
21	chr1:151332600-151336200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:151333200-151336800	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr1:151333400-151333600	Enhancers	Spleen	Spleen
24	chr1:151333600-151334600	Weak transcription	Spleen	Spleen
25	chr1:151333800-151334400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:151333800-151335400	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr1:151334000-151336000	Weak transcription	Left Ventricle	heart
28	chr1:151334000-151336000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr1:151334400-151335600	ZNF genes & repeats	K562	blood
30	chr1:151334400-151336400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:151334400-151341600	Strong transcription	Fetal Lung	lung
32	chr1:151334600-151335000	ZNF genes & repeats	Fetal Kidney	kidney
33	chr1:151334600-151335200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
34	chr1:151334600-151335200	ZNF genes & repeats	Brain Substantia Nigra	brain
35	chr1:151334600-151335200	ZNF genes & repeats	Pancreas	Pancrea
36	chr1:151334600-151335200	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
37	chr1:151334600-151335400	ZNF genes & repeats	Gastric	stomach
38	chr1:151334600-151335400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr1:151334600-151335400	ZNF genes & repeats	Spleen	Spleen
40	chr1:151334600-151335600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr1:151334600-151335600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr1:151334600-151335600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr1:151334600-151335600	ZNF genes & repeats	Adipose Nuclei	Adipose
44	chr1:151334600-151335600	ZNF genes & repeats	Esophagus	oesophagus
45	chr1:151334600-151335600	ZNF genes & repeats	Lung	lung
46	chr1:151334600-151335800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:151334600-151335800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:151334600-151336000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr1:151334600-151336200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
50	chr1:151334600-151337000	ZNF genes & repeats	Fetal Intestine Small	intestine

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