Variant report

Variant	nsv1033597
Chromosome Location	chr5:178423101-178752095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2426)
CpG islands
(count:9344)
Chromatin interactive
region (count:120)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2426 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178614256-178614523	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178570502-178570786	K562	blood:	n/a	n/a
3	ARID3A	chr5:178450529-178450765	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:178435793-178435958	K562	blood:	n/a	n/a
5	ARID3A	chr5:178570524-178570804	HepG2	liver:	n/a	n/a
6	ATF1	chr5:178516546-178516874	K562	blood:	n/a	n/a
7	ATF1	chr5:178729527-178729868	K562	blood:	n/a	n/a
8	ATF1	chr5:178658394-178658571	K562	blood:	n/a	n/a
9	ATF2	chr5:178570450-178570822	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:178688256-178688623	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr5:178570381-178570760	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr5:178516536-178516788	K562	blood:	n/a	chr5:178516689-178516699 chr5:178516688-178516703 chr5:178516689-178516702 chr5:178516691-178516711 chr5:178516692-178516702 chr5:178516688-178516701 chr5:178516690-178516701 chr5:178516692-178516700 chr5:178516692-178516699 chr5:178516690-178516701
13	ATF3	chr5:178570449-178570756	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr5:178587754-178587897	K562	blood:	n/a	n/a
15	BACH1	chr5:178481513-178481613	K562	blood:	n/a	n/a
16	BACH1	chr5:178688361-178688719	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr5:178481413-178481714	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr5:178475617-178476112	GM12878	blood:	n/a	n/a
19	BATF	chr5:178475729-178476166	GM12878	blood:	n/a	n/a
20	BCL11A	chr5:178475718-178476032	GM12878	blood:	n/a	n/a
21	BCL11A	chr5:178475632-178476123	GM12878	blood:	n/a	n/a
22	BCL3	chr5:178650193-178650886	GM12878	blood:	n/a	n/a
23	BCL3	chr5:178746298-178746633	GM12878	blood:	n/a	n/a
24	BCL3	chr5:178746077-178746614	GM12878	blood:	n/a	n/a
25	BCL3	chr5:178650528-178650927	GM12878	blood:	n/a	n/a
26	BHLHE40	chr5:178622593-178622738	K562	blood:	n/a	chr5:178622682-178622695
27	BHLHE40	chr5:178639943-178640216	K562	blood:	n/a	n/a
28	BHLHE40	chr5:178712032-178712059	K562	blood:	n/a	n/a
29	BHLHE40	chr5:178691705-178692905	HepG2	liver:	n/a	chr5:178692685-178692701 chr5:178692599-178692615
30	BHLHE40	chr5:178695327-178695745	HepG2	liver:	n/a	n/a
31	BHLHE40	chr5:178594282-178594482	K562	blood:	n/a	n/a
32	BHLHE40	chr5:178450583-178450973	K562	blood:	n/a	n/a
33	BHLHE40	chr5:178496356-178496412	K562	blood:	n/a	n/a
34	BHLHE40	chr5:178655800-178656133	K562	blood:	n/a	n/a
35	BHLHE40	chr5:178703446-178703646	K562	blood:	n/a	n/a
36	BHLHE40	chr5:178594178-178594361	GM12878	blood:	n/a	chr5:178594259-178594275
37	BHLHE40	chr5:178703014-178703214	K562	blood:	n/a	n/a
38	BHLHE40	chr5:178722893-178723057	K562	blood:	n/a	chr5:178723031-178723040 chr5:178723031-178723040
39	BRCA1	chr5:178487152-178487471	H1-hESC	embryonic stem cell:	n/a	n/a
40	CBX3	chr5:178587627-178587883	K562	blood:	n/a	n/a
41	CBX3	chr5:178729517-178729803	K562	blood:	n/a	n/a
42	CCNT2	chr5:178594142-178594401	K562	blood:	n/a	n/a
43	CCNT2	chr5:178516589-178516784	K562	blood:	n/a	n/a
44	CCNT2	chr5:178450829-178451180	K562	blood:	n/a	n/a
45	CCNT2	chr5:178702918-178703113	K562	blood:	n/a	n/a
46	CEBPB	chr5:178428094-178428259	K562	blood:	n/a	chr5:178428183-178428194
47	CEBPB	chr5:178692615-178693038	HepG2	liver:	n/a	chr5:178692842-178692853
48	CEBPB	chr5:178696901-178697251	IMR90	lung:	n/a	n/a
49	CEBPB	chr5:178692736-178692932	K562	blood:	n/a	chr5:178692842-178692853
50	CEBPB	chr5:178692543-178693542	IMR90	lung:	n/a	chr5:178692842-178692853

(count:9344 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178667819-178667869	H1-hESC	embryonic stem cell:	embryo
2	chr5:178667819-178667869	IMR90	lung:	fetal
3	chr5:178594990-178595040	GM06990	blood:	n/a
4	chr5:178483871-178483921	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:178598142-178598192	Jurkat	blood:	n/a
6	chr5:178423309-178423359	LNCaP	prostate:	n/a
7	chr5:178592153-178592203	HCT-116	colon:	n/a
8	chr5:178577498-178577548	ProgFib	skin:	n/a
9	chr5:178593924-178593974	GM06990	blood:	n/a
10	chr5:178712051-178712101	AG04449	skin:	fetal
11	chr5:178654006-178654056	HepG2	liver:	n/a
12	chr5:178667819-178667869	H1-hESC	embryonic stem cell:	embryo
13	chr5:178667819-178667869	IMR90	lung:	fetal
14	chr5:178594990-178595040	GM06990	blood:	n/a
15	chr5:178483871-178483921	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:178598142-178598192	Jurkat	blood:	n/a
17	chr5:178423309-178423359	LNCaP	prostate:	n/a
18	chr5:178592153-178592203	HCT-116	colon:	n/a
19	chr5:178577498-178577548	ProgFib	skin:	n/a
20	chr5:178593924-178593974	GM06990	blood:	n/a
21	chr5:178712051-178712101	AG04449	skin:	fetal
22	chr5:178654006-178654056	HepG2	liver:	n/a
23	chr5:178452979-178453029	NHBE	bronchial:	n/a
24	chr5:178450758-178450808	PrEC	prostate:	n/a
25	chr5:178548700-178548750	BJ	skin:	n/a
26	chr5:178487485-178487535	CMK	blood:	n/a
27	chr5:178636918-178636968	CMK	blood:	n/a
28	chr5:178632502-178632552	RPTEC	kidney:	n/a
29	chr5:178423163-178423213	NT2-D1	testis:	n/a
30	chr5:178478137-178478187	SAEC	small airway:	n/a
31	chr5:178487310-178487360	GM19239	blood:	n/a
32	chr5:178423163-178423213	HEEpiC	esophagus:	n/a
33	chr5:178684652-178684702	ProgFib	skin:	n/a
34	chr5:178654006-178654056	SKMC	muscle:	n/a
35	chr5:178612523-178612573	NB4	blood:	n/a
36	chr5:178450595-178450645	BJ	skin:	n/a
37	chr5:178488100-178488150	AG09309	skin:	n/a
38	chr5:178450457-178450507	NHDF-neo	bronchial:	n/a
39	chr5:178702842-178702892	AoSMC	blood vessel:	n/a
40	chr5:178622803-178622853	PANC-1	pancreas:	n/a
41	chr5:178656269-178656319	AG09319	gingival:	n/a
42	chr5:178704915-178704965	Hela-S3	cervix:	n/a
43	chr5:178684000-178684050	AG10803	skin:	n/a
44	chr5:178546095-178546145	HRE	kidney:	n/a
45	chr5:178688308-178688358	PFSK-1	brain:	n/a
46	chr5:178655042-178655092	NB4	blood:	n/a
47	chr5:178545514-178545564	Caco-2	colon:	n/a
48	chr5:178622572-178622622	MCF-7	breast:	n/a
49	chr5:178650512-178650562	RPTEC	kidney:	n/a
50	chr5:178593785-178593835	HRE	kidney:	n/a

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:178650071..178651966-chr5:178658345..178660809,2	MCF-7	breast:
2	chr5:178542353..178545239-chr5:178546502..178548105,2	K562	blood:
3	chr5:178549170..178551463-chr5:178552754..178555057,2	K562	blood:
4	chr5:178433803..178435714-chr5:178438411..178439911,2	MCF-7	breast:
5	chr5:178639654..178640533-chr5:178687929..178688900,5	MCF-7	breast:
6	chr5:178694614..178696834-chr5:178698467..178700770,2	K562	blood:
7	chr5:178559035..178560886-chr5:178563328..178565903,2	K562	blood:
8	chr5:178650071..178651966-chr5:178658345..178660809,2	MCF-7	breast:
9	chr5:178486677..178489431-chr5:178490895..178493650,2	MCF-7	breast:
10	chr5:178508305..178510572-chr5:178515516..178518368,2	K562	blood:
11	chr5:178464139..178466564-chr5:178484015..178485914,2	K562	blood:
12	chr5:178694614..178696474-chr5:178699270..178701166,2	K562	blood:
13	chr5:178631257..178632902-chr5:178635722..178638591,2	K562	blood:
14	chr5:178488531..178490916-chr5:178493267..178496128,2	MCF-7	breast:
15	chr5:178547111..178548845-chr5:178551796..178553713,2	K562	blood:
16	chr5:178559035..178560886-chr5:178563328..178565903,2	K562	blood:
17	chr5:178219952..178220766-chr5:178688074..178688887,3	MCF-7	breast:
18	chr5:178570203..178571201-chr5:178687913..178688718,3	MCF-7	breast:
19	chr5:178626882..178628440-chr5:178635586..178638472,2	MCF-7	breast:
20	chr1:149223934..149224436-chr5:178546980..178547500,3	MCF-7	breast:
21	chr5:178451565..178453293-chr5:178455866..178457677,2	MCF-7	breast:
22	chr3:64008784..64009514-chr5:178540831..178541760,2	MCF-7	breast:
23	chr5:178451565..178453293-chr5:178455866..178457677,2	MCF-7	breast:
24	chr1:149223402..149225514-chr5:178546980..178548500,3	MCF-7	breast:
25	chr5:178669101..178670915-chr5:178673147..178675746,2	MCF-7	breast:
26	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
27	chr5:178698907..178700648-chr5:178703533..178706246,2	MCF-7	breast:
28	chr5:178595920..178597681-chr5:178605368..178607876,2	MCF-7	breast:
29	chr5:178579999..178581669-chr5:178587423..178589774,2	MCF-7	breast:
30	chr5:178694647..178697268-chr5:179049140..179050881,2	MCF-7	breast:
31	chr5:178487796..178490140-chr5:178490313..178493225,2	MCF-7	breast:
32	chr5:178547111..178548841-chr5:178551234..178553296,2	K562	blood:
33	chr5:178256899..178257517-chr5:178489612..178490272,2	K562	blood:
34	chr5:178286798..178288918-chr5:178487242..178488938,2	MCF-7	breast:
35	chr5:178450308..178453089-chr5:178453235..178455700,3	MCF-7	breast:
36	chr5:178650614..178652876-chr5:178653305..178655920,2	K562	blood:
37	chr5:178450567..178452511-chr5:178457855..178459672,2	MCF-7	breast:
38	chr5:178487796..178490140-chr5:178490313..178493225,2	MCF-7	breast:
39	chr5:178570556..178571105-chr5:178687987..178688905,2	MCF-7	breast:
40	chr5:178547111..178548841-chr5:178551234..178553296,2	K562	blood:
41	chr5:178649094..178651976-chr5:178660819..178662665,2	MCF-7	breast:
42	chr5:178547111..178548845-chr5:178551796..178553713,2	K562	blood:
43	chr5:178599047..178601683-chr5:178602682..178604778,3	K562	blood:
44	chr5:178669101..178670915-chr5:178673147..178675746,2	MCF-7	breast:
45	chr5:178694614..178696834-chr5:178698467..178700770,2	K562	blood:
46	chr5:178605312..178606812-chr7:157081682..157083546,2	MCF-7	breast:
47	chr5:178583720..178585825-chr5:178586641..178588375,2	K562	blood:
48	chr5:178445660..178448153-chr5:178448435..178450460,2	MCF-7	breast:
49	chr5:178595920..178597681-chr5:178605368..178607876,2	MCF-7	breast:
50	chr5:178445660..178448153-chr5:178448435..178450460,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM6-3	chr5:178424970-178425816	NONHSAT105570
2	lnc-GRM6-4	chr5:178537854-178540736	NONHSAT105574
3	lnc-GRM6-2	chr5:178422897-178423207	NONHSAT105569
4	lnc-GRM6-4	chr5:178537868-178539359	NONHSAT105575

No data

Variant related genes	Relation type
ENSG00000253144	TF binding region
ADAMTS2	TF binding region
ENSG00000254158	TF binding region
ZNF879	TF binding region
GRM6	TF binding region
ZNF354C	TF binding region
ENSG00000253144	CpG island
ADAMTS2	CpG island
ENSG00000254158	CpG island
ZNF879	CpG island
GRM6	CpG island
ZNF354C	CpG island
ENSG00000177932	chromatin interactions
ENSG00000178338	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000113262	chromatin interactions
ENSG00000087116	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000234284	chromatin interactions
ENSG00000253144	chromatin interactions
ENSG00000163636	chromatin interactions

Extended variants
information (count: 13816 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:13816 , 50 per page) page: 1 2 3 4 5 6 7 ... 277

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185555609	chr5:178423115-178423116	Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs373311549	chr5:178423219-178423220	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190317915	chr5:178423224-178423225	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs372054063	chr5:178423257-178423258	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540240916	chr5:178423283-178423284	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs565028387	chr5:178423289-178423290	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532514300	chr5:178423353-178423354	Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs180775650	chr5:178423365-178423366	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568989263	chr5:178423376-178423377	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577464840	chr5:178423395-178423396	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs529912202	chr5:178423417-178423418	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185437269	chr5:178423418-178423419	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566770237	chr5:178423436-178423437	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533763814	chr5:178423460-178423461	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs539533979	chr5:178423474-178423475	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570542501	chr5:178423494-178423495	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs542805408	chr5:178423495-178423496	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs537974282	chr5:178423516-178423517	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs116065883	chr5:178423517-178423518	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575721248	chr5:178423520-178423521	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs3756565	chr5:178423569-178423570	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs554922973	chr5:178423571-178423572	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs73804517	chr5:178423572-178423573	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs559627690	chr5:178423584-178423585	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs116631972	chr5:178423602-178423603	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576909129	chr5:178423621-178423622	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs544343036	chr5:178423635-178423636	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114077740	chr5:178423636-178423637	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs529812033	chr5:178423724-178423725	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs145482903	chr5:178423795-178423796	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs548408142	chr5:178423798-178423799	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs560465254	chr5:178423799-178423800	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs3756564	chr5:178423803-178423804	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552187213	chr5:178423817-178423818	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs3756563	chr5:178423820-178423821	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs537861907	chr5:178423833-178423834	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192244556	chr5:178423849-178423850	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs568157207	chr5:178423856-178423857	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs536434061	chr5:178423864-178423865	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528178813	chr5:178423865-178423866	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs546413370	chr5:178423872-178423873	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs573177691	chr5:178423980-178423981	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs112512272	chr5:178424013-178424014	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs558836321	chr5:178424022-178424023	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs368174640	chr5:178424040-178424041	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs184079093	chr5:178424071-178424072	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs114074036	chr5:178424079-178424080	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562834835	chr5:178424081-178424082	Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs574925488	chr5:178424108-178424109	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs73338556	chr5:178424124-178424125	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:5541 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178422400-178423400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:178422600-178423200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
3	chr5:178422600-178423400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
4	chr5:178422600-178424200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:178423000-178423200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:178423200-178423400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
7	chr5:178436200-178436400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr5:178439600-178440000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
9	chr5:178442200-178443200	ZNF genes & repeats	Liver	Liver
10	chr5:178448400-178450200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:178449600-178449800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr5:178449600-178451600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:178449800-178450000	ZNF genes & repeats	Liver	Liver
14	chr5:178449800-178450200	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr5:178449800-178450200	Enhancers	HUVEC	blood vessel
16	chr5:178449800-178451000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
17	chr5:178449800-178451200	Active TSS	Brain Anterior Caudate	brain
18	chr5:178449800-178451200	Active TSS	Skeletal Muscle Male	skeletal muscle
19	chr5:178449800-178451400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr5:178449800-178451400	Active TSS	Skeletal Muscle Female	skeletal muscle
21	chr5:178449800-178451600	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr5:178449800-178451600	Active TSS	H1 Cell Line	embryonic stem cell
23	chr5:178449800-178451600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr5:178449800-178451600	Active TSS	Duodenum Smooth Muscle	Duodenum
25	chr5:178449800-178451800	Active TSS	HMEC	breast
26	chr5:178449800-178452000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr5:178449800-178452000	Active TSS	Psoas Muscle	Psoas
28	chr5:178450000-178450200	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr5:178450000-178450200	Bivalent/Poised TSS	Primary B cells from cord blood	blood
30	chr5:178450000-178450200	Enhancers	Primary B cells from peripheral blood	blood
31	chr5:178450000-178450200	Active TSS	Primary T cells fromperipheralblood	blood
32	chr5:178450000-178450200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr5:178450000-178450200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr5:178450000-178450200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:178450000-178450200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
36	chr5:178450000-178450200	Active TSS	Fetal Muscle Trunk	muscle
37	chr5:178450000-178451000	Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr5:178450000-178451200	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr5:178450000-178451200	Active TSS	Adipose Nuclei	Adipose
40	chr5:178450000-178451200	Active TSS	Fetal Brain Female	brain
41	chr5:178450000-178451400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr5:178450000-178451600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr5:178450000-178451600	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr5:178450000-178451600	Active TSS	Fetal Stomach	stomach
45	chr5:178450000-178451600	Active TSS	Right Atrium	heart
46	chr5:178450000-178451800	Active TSS	H9 Cell Line	embryonic stem cell
47	chr5:178450000-178452200	Active TSS	Duodenum Mucosa	Duodenum
48	chr5:178450000-178452200	Active TSS	Fetal Kidney	kidney
49	chr5:178450200-178450400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr5:178450200-178450400	Active TSS	Primary T helper cells fromperipheralblood	blood

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