Variant report

Variant	nsv537052
Chromosome Location	chr4:20601908-21057992
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:20692322-20692456	K562	blood:	n/a	n/a
2	ARID3A	chr4:20775077-20775342	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:20701592-20701812	K562	blood:	n/a	n/a
4	ARID3A	chr4:20701873-20702300	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:20700015-20700842	K562	blood:	n/a	n/a
6	ATF1	chr4:20865610-20865795	K562	blood:	n/a	n/a
7	ATF1	chr4:20701653-20702260	K562	blood:	n/a	chr4:20702025-20702039
8	ATF1	chr4:20700407-20700806	K562	blood:	n/a	n/a
9	ATF2	chr4:20701648-20702230	H1-hESC	embryonic stem cell:	n/a	chr4:20702025-20702039
10	ATF3	chr4:20701734-20702174	GM12878	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
11	ATF3	chr4:20700358-20700813	K562	blood:	n/a	n/a
12	ATF3	chr4:20701711-20702195	HepG2	liver:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
13	ATF3	chr4:20701697-20702170	H1-hESC	embryonic stem cell:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
14	ATF3	chr4:20701739-20702217	K562	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
15	ATF3	chr4:20701812-20702063	GM12878	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
16	ATF3	chr4:20701701-20702121	K562	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
17	ATF3	chr4:20701755-20702123	H1-hESC	embryonic stem cell:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
18	ATF3	chr4:20701728-20702041	A549	lung:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
19	BACH1	chr4:20817391-20817392	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:20985747-20986024	H1-hESC	embryonic stem cell:	n/a	n/a
21	BHLHE40	chr4:20700392-20700749	K562	blood:	n/a	n/a
22	BHLHE40	chr4:20688384-20688430	K562	blood:	n/a	n/a
23	BHLHE40	chr4:20726709-20727073	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:20686889-20687054	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:20627171-20627455	K562	blood:	n/a	n/a
26	BHLHE40	chr4:20701761-20702364	HepG2	liver:	n/a	n/a
27	BHLHE40	chr4:20775048-20775386	HepG2	liver:	n/a	n/a
28	BHLHE40	chr4:20811465-20811810	HepG2	liver:	n/a	n/a
29	BHLHE40	chr4:20701625-20702344	K562	blood:	n/a	n/a
30	BHLHE40	chr4:20701479-20702280	GM12878	blood:	n/a	n/a
31	BRCA1	chr4:20701812-20702075	HepG2	liver:	n/a	n/a
32	BRCA1	chr4:20701819-20702207	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr4:20686884-20687072	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr4:20701588-20702105	K562	blood:	n/a	n/a
35	CCNT2	chr4:20700385-20700870	K562	blood:	n/a	n/a
36	CCNT2	chr4:20701740-20702316	K562	blood:	n/a	n/a
37	CCNT2	chr4:21050255-21050426	K562	blood:	n/a	n/a
38	CEBPB	chr4:20733820-20734122	IMR90	lung:	n/a	chr4:20733957-20733968
39	CEBPB	chr4:20701891-20702151	K562	blood:	n/a	n/a
40	CEBPB	chr4:20622154-20622294	A549	lung:	n/a	chr4:20622207-20622216 chr4:20622205-20622218 chr4:20622205-20622216 chr4:20622207-20622216 chr4:20622207-20622216 chr4:20622207-20622216
41	CEBPB	chr4:20800556-20800817	HepG2	liver:	n/a	chr4:20800688-20800699 chr4:20800653-20800664
42	CEBPB	chr4:20836373-20836591	IMR90	lung:	n/a	n/a
43	CEBPB	chr4:20700088-20700367	K562	blood:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
44	CEBPB	chr4:20836338-20836538	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:20741665-20741893	K562	blood:	n/a	n/a
46	CEBPB	chr4:21007315-21007659	HepG2	liver:	n/a	chr4:21007478-21007489 chr4:21007479-21007488 chr4:21007479-21007488 chr4:21007477-21007490 chr4:21007479-21007488
47	CEBPB	chr4:20699982-20700715	K562	blood:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
48	CEBPB	chr4:20797109-20797407	HepG2	liver:	n/a	chr4:20797259-20797272 chr4:20797259-20797270
49	CEBPB	chr4:21016785-21016985	HepG2	liver:	n/a	chr4:21016833-21016844
50	CEBPB	chr4:21016698-21016997	IMR90	lung:	n/a	chr4:21016833-21016844

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:20884431-20884481	Caco-2	colon:	n/a
2	chr4:20884321-20884371	NB4	blood:	n/a
3	chr4:20884321-20884371	HEK293	kidney:	embryo
4	chr4:20852672-20852722	HRPEpiC	eye:	n/a
5	chr4:21004400-21004450	NH-A	brain:	n/a
6	chr4:20884431-20884481	Caco-2	colon:	n/a
7	chr4:20884321-20884371	NB4	blood:	n/a
8	chr4:20884321-20884371	HEK293	kidney:	embryo
9	chr4:20852672-20852722	HRPEpiC	eye:	n/a
10	chr4:21004400-21004450	NH-A	brain:	n/a
11	chr4:20811042-20811092	Jurkat	blood:	n/a
12	chr4:20701950-20702000	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:20985984-20986034	NHDF-neo	bronchial:	n/a
14	chr4:20985927-20985977	ProgFib	skin:	n/a
15	chr4:20706485-20706535	MCF10A-Er-Src	breast:	n/a
16	chr4:20701950-20702000	SKMC	muscle:	n/a
17	chr4:21004400-21004450	NB4	blood:	n/a
18	chr4:20701950-20702000	K562	blood:	n/a
19	chr4:20852672-20852722	HEK293	kidney:	embryo
20	chr4:20702045-20702095	AG04450	lung:	fetal
21	chr4:20701889-20701939	HCF	heart:	n/a
22	chr4:20702045-20702095	ovcar-3	ovarian:	n/a
23	chr4:20985927-20985977	HCF	heart:	n/a
24	chr4:20884321-20884371	GM12878	blood:	n/a
25	chr4:20701925-20701975	AG09319	gingival:	n/a
26	chr4:20698772-20698822	GM19239	blood:	n/a
27	chr4:20885536-20885586	SAEC	small airway:	n/a
28	chr4:20852366-20852416	T-47D	breast:	n/a
29	chr4:20960712-20960762	PrEC	prostate:	n/a
30	chr4:20730493-20730543	GM12892	blood:	n/a
31	chr4:20730493-20730543	NT2-D1	testis:	n/a
32	chr4:20698772-20698822	Jurkat	blood:	n/a
33	chr4:20811042-20811092	MCF-7	breast:	n/a
34	chr4:20885536-20885586	HNPCEpiC	eye:	n/a
35	chr4:20988275-20988325	Hepatocyte	liver:	n/a
36	chr4:21039877-21039927	PFSK-1	brain:	n/a
37	chr4:20884321-20884371	GM06990	blood:	n/a
38	chr4:20985927-20985977	AG09309	skin:	n/a
39	chr4:20698772-20698822	GM12892	blood:	n/a
40	chr4:20852337-20852387	HEEpiC	esophagus:	n/a
41	chr4:20985984-20986034	MCF10A-Er-Src	breast:	n/a
42	chr4:20885536-20885586	IMR90	lung:	fetal
43	chr4:20985984-20986034	K562	blood:	n/a
44	chr4:20704940-20704990	ProgFib	skin:	n/a
45	chr4:20701914-20701964	GM12891	blood:	n/a
46	chr4:20885536-20885586	PrEC	prostate:	n/a
47	chr4:20852366-20852416	BE2_C	brain:	n/a
48	chr4:20698772-20698822	HCT-116	colon:	n/a
49	chr4:20701914-20701964	SAEC	small airway:	n/a
50	chr4:20811042-20811092	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:20423749..20424719-chr4:20686427..20687473,4	K562	blood:
2	chr4:20758225..20761110-chr4:20761707..20763289,2	MCF-7	breast:
3	chr4:20774939..20775520-chr4:21136553..21137202,2	MCF-7	breast:
4	chr4:20791958..20793489-chr4:20799634..20802311,2	K562	blood:
5	chr4:20759824..20762284-chr4:20763447..20765411,2	K562	blood:
6	chr4:20791958..20793489-chr4:20799634..20802311,2	K562	blood:
7	chr4:20971332..20974110-chr4:20975805..20978136,2	K562	blood:
8	chr4:20779088..20780993-chr4:20896835..20899396,2	K562	blood:
9	chr4:20699912..20701731-chr4:20714831..20716673,2	K562	blood:
10	chr4:20702272..20703966-chr4:20709575..20711144,2	MCF-7	breast:
11	chr4:20776494..20778419-chr4:20785252..20787706,2	K562	blood:
12	chr4:20647329..20649016-chr4:20649617..20652093,2	K562	blood:
13	chr4:20756151..20758021-chr4:20765219..20767901,2	K562	blood:
14	chr4:20756151..20758021-chr4:20765219..20767901,2	K562	blood:
15	chr4:20650338..20652484-chr4:20652879..20655131,2	K562	blood:
16	chr1:147804723..147806420-chr4:20979153..20981320,2	MCF-7	breast:
17	chr4:20702888..20705883-chr4:20707634..20710929,3	K562	blood:
18	chr4:20693086..20698959-chr4:20699230..20704175,9	K562	blood:
19	chr4:20650338..20652484-chr4:20652879..20655131,2	K562	blood:
20	chr4:21002667..21005415-chr4:21005443..21008347,2	K562	blood:
21	chr4:20700245..20702604-chr4:20707211..20709448,2	MCF-7	breast:
22	chr4:20700229..20702940-chr4:20728046..20730028,2	MCF-7	breast:
23	chr4:20940626..20942127-chr4:20945526..20948025,2	K562	blood:
24	chr4:20758225..20761110-chr4:20761707..20763289,2	MCF-7	breast:
25	chr4:20702272..20703966-chr4:20709575..20711144,2	MCF-7	breast:
26	chr4:20424367..20425209-chr4:20686856..20687583,2	MCF-7	breast:
27	chr4:20736150..20738048-chr4:20747130..20748840,2	K562	blood:
28	chr4:20966569..20968200-chr4:20971149..20973804,2	K562	blood:
29	chr4:20705332..20707768-chr4:20710083..20712545,3	K562	blood:
30	chr4:20736248..20737799-chr4:20738056..20739802,2	MCF-7	breast:
31	chr4:20940626..20942127-chr4:20945526..20948025,2	K562	blood:
32	chr4:20701536..20702331-chr9:91933301..91933855,2	Hela-S3	cervix:
33	chr4:20779088..20780993-chr4:20896835..20899396,2	K562	blood:
34	chr4:20700439..20703043-chr4:20709421..20711457,2	MCF-7	breast:
35	chr4:20736248..20737799-chr4:20738056..20739802,2	MCF-7	breast:
36	chr4:20736150..20738048-chr4:20747130..20748840,2	K562	blood:
37	chr4:20774749..20775678-chr4:21136384..21137379,5	MCF-7	breast:
38	chr4:20733613..20735469-chr4:20737753..20739786,2	K562	blood:
39	chr4:20702290..20704847-chr4:20728043..20731005,3	K562	blood:
40	chr4:20700245..20702604-chr4:20707211..20709448,2	MCF-7	breast:
41	chr4:20705332..20707768-chr4:20710083..20712545,3	K562	blood:
42	chr4:20966569..20968200-chr4:20971149..20973804,2	K562	blood:
43	chr4:20700439..20703043-chr4:20709421..20711457,2	MCF-7	breast:
44	chr4:20702290..20704847-chr4:20728043..20731005,3	K562	blood:
45	chr4:20776494..20778419-chr4:20785252..20787706,2	K562	blood:
46	chr4:20774692..20775734-chr4:21470776..21471557,3	MCF-7	breast:
47	chr4:20702290..20703806-chr4:20728599..20731005,2	K562	blood:
48	chr4:20699912..20701731-chr4:20714831..20716673,2	K562	blood:
49	chr4:20971332..20974110-chr4:20975805..20978136,2	K562	blood:
50	chr4:20678463..20679308-chr6:4856088..4856696,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLIT2-2	chr4:20702061-20702329	NONHSAT095736
2	lnc-SLIT2-3	chr4:20733323-20734177	NONHSAT095738
3	lnc-SLIT2-3	chr4:20731428-20733259	NONHSAT095738
4	lnc-SLIT2-2	chr4:20704298-20704317	NONHSAT095736
5	lnc-PACRGL-6	chr4:20768431-20768995	ENSG00000272995.1
6	lnc-SLIT2-2	chr4:20703764-20703844	NONHSAT095736
7	lnc-SLIT2-2	chr4:20703381-20703507	NONHSAT095736

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PACRGL	hsa-miR-373-3p	chr4:20754297-20754319

Variant related genes	Relation type
KCNIP4	TF binding region
SLIT2	TF binding region
ENSG00000272995	TF binding region
PACRGL	TF binding region
KCNIP4	CpG island
SLIT2	CpG island
ENSG00000272995	CpG island
PACRGL	CpG island
ENSG00000163138	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000135596	chromatin interactions

Extended variants
information (count: 13597 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:13597 , 50 per page) page: 1 2 3 4 5 6 7 ... 272

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201477744	chr4:20601949-20601950	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114113277	chr4:20601952-20601953	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78328514	chr4:20601954-20601955	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530638799	chr4:20602001-20602002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548668120	chr4:20602026-20602027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200048770	chr4:20602035-20602036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201170857	chr4:20602037-20602038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7654670	chr4:20602038-20602039	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs13102137	chr4:20602039-20602040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555077466	chr4:20602048-20602049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531922475	chr4:20602108-20602109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374118750	chr4:20602109-20602110	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189185754	chr4:20602163-20602164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546921282	chr4:20602172-20602173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113937782	chr4:20602182-20602183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538889751	chr4:20602186-20602187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142309232	chr4:20602196-20602197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545279776	chr4:20602215-20602216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568971950	chr4:20602237-20602238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536770075	chr4:20602248-20602249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554640665	chr4:20602255-20602256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573219717	chr4:20602278-20602279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534598665	chr4:20602392-20602393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78310442	chr4:20602426-20602427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553345212	chr4:20602456-20602457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577910570	chr4:20602460-20602461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112767735	chr4:20602472-20602473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563489652	chr4:20602505-20602506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565085503	chr4:20602576-20602577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563284503	chr4:20602591-20602592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146333002	chr4:20602634-20602635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139010390	chr4:20602696-20602697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574291401	chr4:20602715-20602716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528128091	chr4:20602746-20602747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527461210	chr4:20602749-20602750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565189060	chr4:20602774-20602775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7660834	chr4:20602810-20602811	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs149355386	chr4:20602826-20602827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114901182	chr4:20602891-20602892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536329239	chr4:20602944-20602945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377666530	chr4:20602961-20602962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548698492	chr4:20602970-20602971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566744938	chr4:20603002-20603003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534232592	chr4:20603003-20603004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115140635	chr4:20603011-20603012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530140600	chr4:20603025-20603026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187270344	chr4:20603028-20603029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190876559	chr4:20603031-20603032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538955815	chr4:20603139-20603140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557169416	chr4:20603153-20603154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20531469	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3029 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20536800-20618600	Weak transcription	Spleen	Spleen
2	chr4:20567000-20604000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:20567200-20605200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr4:20567200-20617000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr4:20578000-20617400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr4:20578200-20616800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:20578400-20610000	Weak transcription	Fetal Brain Male	brain
8	chr4:20579400-20605600	Weak transcription	Adipose Nuclei	Adipose
9	chr4:20589200-20610600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr4:20589200-20620800	Weak transcription	Fetal Muscle Leg	muscle
11	chr4:20590000-20620400	Weak transcription	Fetal Muscle Trunk	muscle
12	chr4:20590800-20618400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr4:20591400-20617000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr4:20591600-20605200	Weak transcription	NHEK	skin
15	chr4:20593000-20619000	Weak transcription	Placenta	Placenta
16	chr4:20594400-20619000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr4:20594600-20602600	Weak transcription	Fetal Intestine Large	intestine
18	chr4:20594600-20605200	Weak transcription	NHLF	lung
19	chr4:20594800-20603800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:20594800-20620600	Weak transcription	Brain Cingulate Gyrus	brain
21	chr4:20595000-20605400	Strong transcription	NHDF-Ad	bronchial
22	chr4:20595800-20604800	Weak transcription	Brain Anterior Caudate	brain
23	chr4:20596800-20605200	Weak transcription	HUVEC	blood vessel
24	chr4:20597800-20624600	Weak transcription	Brain Hippocampus Middle	brain
25	chr4:20598400-20605400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr4:20598400-20615000	Weak transcription	Fetal Stomach	stomach
27	chr4:20598600-20619200	Weak transcription	Ovary	ovary
28	chr4:20600400-20602800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr4:20600400-20614800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:20600400-20619000	Weak transcription	Fetal Kidney	kidney
31	chr4:20600600-20610600	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr4:20600600-20617200	Weak transcription	Aorta	Aorta
33	chr4:20600800-20603000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:20600800-20604800	Weak transcription	Osteobl	bone
35	chr4:20600800-20614800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr4:20600800-20616600	Weak transcription	Colon Smooth Muscle	Colon
37	chr4:20600800-20619000	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr4:20601600-20602000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr4:20601600-20602600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:20601600-20602600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:20601600-20602800	Weak transcription	Fetal Lung	lung
42	chr4:20602600-20603400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:20602600-20605800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:20602800-20604600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr4:20602800-20605200	Strong transcription	Fetal Lung	lung
46	chr4:20603000-20604800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr4:20603400-20604800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:20603800-20605200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:20604000-20605000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:20604600-20617000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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