Variant report

Variant	nsv600496
Chromosome Location	chr5:178552518-178752351
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1748)
CpG islands
(count:6048)
Chromatin interactive
region (count:72)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1748 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

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	chr5:178570524-178570804	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178570502-178570786	K562	blood:	n/a	n/a
4	ATF1	chr5:178729527-178729868	K562	blood:	n/a	n/a
5	ATF1	chr5:178658394-178658571	K562	blood:	n/a	n/a
6	ATF2	chr5:178688256-178688623	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:178570450-178570822	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:178570381-178570760	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr5:178570449-178570756	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr5:178587754-178587897	K562	blood:	n/a	n/a
11	BACH1	chr5:178688361-178688719	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr5:178650193-178650886	GM12878	blood:	n/a	n/a
13	BCL3	chr5:178650528-178650927	GM12878	blood:	n/a	n/a
14	BCL3	chr5:178746298-178746633	GM12878	blood:	n/a	n/a
15	BCL3	chr5:178746077-178746614	GM12878	blood:	n/a	n/a
16	BHLHE40	chr5:178594178-178594361	GM12878	blood:	n/a	chr5:178594259-178594275
17	BHLHE40	chr5:178639943-178640216	K562	blood:	n/a	n/a
18	BHLHE40	chr5:178712032-178712059	K562	blood:	n/a	n/a
19	BHLHE40	chr5:178703014-178703214	K562	blood:	n/a	n/a
20	BHLHE40	chr5:178691705-178692905	HepG2	liver:	n/a	chr5:178692685-178692701 chr5:178692599-178692615
21	BHLHE40	chr5:178655800-178656133	K562	blood:	n/a	n/a
22	BHLHE40	chr5:178703446-178703646	K562	blood:	n/a	n/a
23	BHLHE40	chr5:178722893-178723057	K562	blood:	n/a	chr5:178723031-178723040 chr5:178723031-178723040
24	BHLHE40	chr5:178695327-178695745	HepG2	liver:	n/a	n/a
25	BHLHE40	chr5:178594282-178594482	K562	blood:	n/a	n/a
26	BHLHE40	chr5:178622593-178622738	K562	blood:	n/a	chr5:178622682-178622695
27	CBX3	chr5:178729517-178729803	K562	blood:	n/a	n/a
28	CBX3	chr5:178587627-178587883	K562	blood:	n/a	n/a
29	CCNT2	chr5:178702918-178703113	K562	blood:	n/a	n/a
30	CCNT2	chr5:178594142-178594401	K562	blood:	n/a	n/a
31	CEBPB	chr5:178688334-178688561	K562	blood:	n/a	n/a
32	CEBPB	chr5:178734831-178734994	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:178688296-178688593	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr5:178692707-178692953	Hela-S3	cervix:	n/a	chr5:178692842-178692853
35	CEBPB	chr5:178731436-178731883	IMR90	lung:	n/a	n/a
36	CEBPB	chr5:178749384-178749670	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:178692660-178693031	HepG2	liver:	n/a	chr5:178692842-178692853
38	CEBPB	chr5:178695368-178695660	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:178628227-178628571	IMR90	lung:	n/a	chr5:178628403-178628414
40	CEBPB	chr5:178688337-178688527	K562	blood:	n/a	n/a
41	CEBPB	chr5:178688305-178688589	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:178688281-178688621	IMR90	lung:	n/a	n/a
43	CEBPB	chr5:178648617-178648858	HepG2	liver:	n/a	chr5:178648732-178648743
44	CEBPB	chr5:178628252-178628543	Hela-S3	cervix:	n/a	chr5:178628403-178628414
45	CEBPB	chr5:178628311-178628506	A549	lung:	n/a	chr5:178628403-178628414
46	CEBPB	chr5:178692719-178693033	ECC-1	luminal epithelium:	n/a	chr5:178692842-178692853
47	CEBPB	chr5:178691969-178692038	HepG2	liver:	n/a	n/a
48	CEBPB	chr5:178692615-178693038	HepG2	liver:	n/a	chr5:178692842-178692853
49	CEBPB	chr5:178695431-178695549	HepG2	liver:	n/a	n/a
50	CEBPB	chr5:178696901-178697251	IMR90	lung:	n/a	n/a

(count:6048 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178631741-178631791	K562	blood:	n/a
2	chr5:178692806-178692856	IMR90	lung:	fetal
3	chr5:178654006-178654056	Hepatocyte	liver:	n/a
4	chr5:178631497-178631547	T-47D	breast:	n/a
5	chr5:178651519-178651569	NHBE	bronchial:	n/a
6	chr5:178565001-178565051	SK-N-SH_RA	brain:	n/a
7	chr5:178692728-178692778	BE2_C	brain:	n/a
8	chr5:178631497-178631547	AoSMC	blood vessel:	n/a
9	chr5:178577498-178577548	NHDF-neo	bronchial:	n/a
10	chr5:178631741-178631791	K562	blood:	n/a
11	chr5:178692806-178692856	IMR90	lung:	fetal
12	chr5:178654006-178654056	Hepatocyte	liver:	n/a
13	chr5:178631497-178631547	T-47D	breast:	n/a
14	chr5:178651519-178651569	NHBE	bronchial:	n/a
15	chr5:178565001-178565051	SK-N-SH_RA	brain:	n/a
16	chr5:178692728-178692778	BE2_C	brain:	n/a
17	chr5:178631497-178631547	AoSMC	blood vessel:	n/a
18	chr5:178577498-178577548	NHDF-neo	bronchial:	n/a
19	chr5:178687826-178687876	HCPEpiC	choroid plexus:	n/a
20	chr5:178654006-178654056	AG09309	skin:	n/a
21	chr5:178564818-178564868	HL-60	blood:	n/a
22	chr5:178622080-178622130	SAEC	small airway:	n/a
23	chr5:178554242-178554292	GM12891	blood:	n/a
24	chr5:178636918-178636968	HCPEpiC	choroid plexus:	n/a
25	chr5:178567126-178567176	GM12878	blood:	n/a
26	chr5:178632502-178632552	NHDF-neo	bronchial:	n/a
27	chr5:178553496-178553546	HPAEpiC	pulmonary alveolar:	n/a
28	chr5:178622080-178622130	ECC-1	luminal epithelium:	n/a
29	chr5:178741283-178741333	SK-N-MC	brain:	n/a
30	chr5:178594526-178594576	U87	brain:	n/a
31	chr5:178687984-178688034	HL-60	blood:	n/a
32	chr5:178618678-178618728	GM06990	blood:	n/a
33	chr5:178594447-178594497	K562	blood:	n/a
34	chr5:178667709-178667759	PFSK-1	brain:	n/a
35	chr5:178683834-178683884	SK-N-MC	brain:	n/a
36	chr5:178712084-178712134	NHDF-neo	bronchial:	n/a
37	chr5:178656269-178656319	H1-hESC	embryonic stem cell:	embryo
38	chr5:178697400-178697450	AG04450	lung:	fetal
39	chr5:178632502-178632552	SK-N-MC	brain:	n/a
40	chr5:178591479-178591529	SK-N-SH_RA	brain:	n/a
41	chr5:178622120-178622170	SKMC	muscle:	n/a
42	chr5:178592153-178592203	HRCEpiC	kidney:	n/a
43	chr5:178591479-178591529	HCT-116	colon:	n/a
44	chr5:178594526-178594576	GM19239	blood:	n/a
45	chr5:178592153-178592203	HCPEpiC	choroid plexus:	n/a
46	chr5:178565917-178565967	HUVEC	blood vessel:	n/a
47	chr5:178702842-178702892	HUVEC	blood vessel:	n/a
48	chr5:178614909-178614959	SK-N-MC	brain:	n/a
49	chr5:178632502-178632552	AG09309	skin:	n/a
50	chr5:178623035-178623085	NHDF-neo	bronchial:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:178626882..178628440-chr5:178635586..178638472,2	MCF-7	breast:
2	chr5:178613030..178614553-chr5:178617663..178620440,2	K562	blood:
3	chr5:178579999..178581669-chr5:178587423..178589774,2	MCF-7	breast:
4	chr5:178652878..178655223-chr5:178665952..178668603,2	K562	blood:
5	chr5:178599047..178601683-chr5:178602682..178604778,3	K562	blood:
6	chr5:178687965..178688655-chr5:178920708..178921301,2	K562	blood:
7	chr5:178631257..178632902-chr5:178635722..178638591,2	K562	blood:
8	chr5:178639660..178640480-chr5:178701010..178701947,3	MCF-7	breast:
9	chr5:178619900..178622290-chr5:178622494..178625423,2	MCF-7	breast:
10	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
11	chr5:178669552..178671241-chr5:178672789..178674406,2	K562	blood:
12	chr5:178694614..178696474-chr5:178699270..178701166,2	K562	blood:
13	chr5:178631257..178632902-chr5:178635722..178638591,2	K562	blood:
14	chr5:178570203..178571201-chr5:178687913..178688718,3	MCF-7	breast:
15	chr5:178639660..178640480-chr5:178701010..178701947,3	MCF-7	breast:
16	chr5:178652878..178655223-chr5:178665952..178668603,2	K562	blood:
17	chr5:178650614..178652876-chr5:178653305..178655920,2	K562	blood:
18	chr5:178593773..178595177-chr5:178920715..178921686,6	MCF-7	breast:
19	chr5:178698907..178700648-chr5:178703533..178706246,2	MCF-7	breast:
20	chr5:178486462..178489225-chr5:178551148..178554695,3	MCF-7	breast:
21	chr5:178688082..178688899-chr5:178920410..178921212,2	MCF-7	breast:
22	chr5:178669552..178671241-chr5:178672789..178674406,2	K562	blood:
23	chr5:178570556..178571105-chr5:178687987..178688905,2	MCF-7	breast:
24	chr5:178547111..178548845-chr5:178551796..178553713,2	K562	blood:
25	chr5:178549170..178551463-chr5:178552754..178555057,2	K562	blood:
26	chr5:178545417..178547035-chr5:178698975..178701216,2	K562	blood:
27	chr5:178483751..178486234-chr5:178558590..178560353,2	MCF-7	breast:
28	chr5:178593807..178594987-chr5:178687910..178688845,5	MCF-7	breast:
29	chr5:178613030..178614553-chr5:178617663..178620440,2	K562	blood:
30	chr5:178694614..178696834-chr5:178698467..178700770,2	K562	blood:
31	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
32	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
33	chr5:178605312..178606812-chr7:157081682..157083546,2	MCF-7	breast:
34	chr5:178593807..178594987-chr5:178687910..178688845,5	MCF-7	breast:
35	chr5:178650071..178651966-chr5:178658345..178660809,2	MCF-7	breast:
36	chr5:178606888..178609097-chr5:178620867..178622421,2	MCF-7	breast:
37	chr5:178579999..178581669-chr5:178587423..178589774,2	MCF-7	breast:
38	chr5:178547111..178548841-chr5:178551234..178553296,2	K562	blood:
39	chr5:178673165..178675582-chr5:178682729..178684288,2	MCF-7	breast:
40	chr5:178559035..178560886-chr5:178563328..178565903,2	K562	blood:
41	chr5:178570556..178571105-chr5:178687987..178688905,2	MCF-7	breast:
42	chr5:178650614..178652876-chr5:178653305..178655920,2	K562	blood:
43	chr5:178583720..178585825-chr5:178586641..178588375,2	K562	blood:
44	chr5:178606888..178609097-chr5:178620867..178622421,2	MCF-7	breast:
45	chr5:178694614..178696834-chr5:178698467..178700770,2	K562	blood:
46	chr5:178599047..178601683-chr5:178602682..178604778,3	K562	blood:
47	chr5:178694647..178697268-chr5:179049140..179050881,2	MCF-7	breast:
48	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
49	chr5:178669101..178670915-chr5:178673147..178675746,2	MCF-7	breast:
50	chr5:178694614..178696474-chr5:178699270..178701166,2	K562	blood:

No data

Variant related genes	Relation type
ADAMTS2	TF binding region
ADAMTS2	CpG island
ENSG00000177932	chromatin interactions
ENSG00000087116	chromatin interactions
ENSG00000169045	chromatin interactions

Extended variants
information (count: 9838 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:9838 , 50 per page) page: 1 2 3 4 5 6 7 ... 197

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6860046	chr5:178552518-178552519	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550758053	chr5:178552530-178552531	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs11948229	chr5:178552547-178552548	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs536569764	chr5:178552573-178552574	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs554581438	chr5:178552605-178552606	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572913583	chr5:178552621-178552622	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs533866651	chr5:178552641-178552642	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548066089	chr5:178552657-178552658	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs558416615	chr5:178552683-178552684	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs7718671	chr5:178552715-178552716	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs374686318	chr5:178552727-178552728	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565194804	chr5:178552734-178552735	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147365657	chr5:178552743-178552744	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs61320168	chr5:178552744-178552745	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs542942176	chr5:178552774-178552775	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs10035909	chr5:178552798-178552799	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs183708852	chr5:178552814-178552815	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs528512484	chr5:178552835-178552836	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540623599	chr5:178552862-178552863	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs565192542	chr5:178552890-178552891	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs78566312	chr5:178552899-178552900	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs550471893	chr5:178552900-178552901	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs569098426	chr5:178552936-178552937	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs2303642	chr5:178552956-178552957	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs200247207	chr5:178552981-178552982	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs370736045	chr5:178552982-178552983	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs567635584	chr5:178553007-178553008	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs566474723	chr5:178553015-178553016	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs6869261	chr5:178553019-178553020	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs151261888	chr5:178553022-178553023	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs373304304	chr5:178553028-178553029	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs141654276	chr5:178553029-178553030	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs199617528	chr5:178553030-178553031	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs376035745	chr5:178553037-178553038	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs570418931	chr5:178553052-178553053	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs370747086	chr5:178553061-178553062	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs373964237	chr5:178553068-178553069	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs377397368	chr5:178553074-178553075	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs370686613	chr5:178553115-178553116	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs374211371	chr5:178553116-178553117	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs371021469	chr5:178553121-178553122	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs537968304	chr5:178553138-178553139	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs373506217	chr5:178553152-178553153	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs372108778	chr5:178553158-178553159	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs374351666	chr5:178553174-178553175	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs2303643	chr5:178553185-178553186	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs575472515	chr5:178553223-178553224	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs542911213	chr5:178553264-178553265	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs139553138	chr5:178553278-178553279	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs573208780	chr5:178553279-178553280	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:3550 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178527800-178559800	Weak transcription	HSMM	muscle
2	chr5:178538000-178560400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr5:178538200-178564600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:178545000-178555000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:178545800-178552800	ZNF genes & repeats	Fetal Stomach	stomach
6	chr5:178546000-178554000	Weak transcription	HSMMtube	muscle
7	chr5:178546800-178563200	Strong transcription	Adipose Nuclei	Adipose
8	chr5:178547000-178565400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:178547400-178560200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr5:178547600-178552800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr5:178547600-178552800	ZNF genes & repeats	Spleen	Spleen
12	chr5:178547600-178560200	Strong transcription	Placenta Amnion	Placenta Amnion
13	chr5:178547800-178560400	Strong transcription	Ovary	ovary
14	chr5:178548000-178559800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr5:178548200-178554800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr5:178548600-178570000	Weak transcription	NHDF-Ad	bronchial
17	chr5:178549000-178553600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr5:178549400-178557000	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr5:178549400-178590800	Weak transcription	Stomach Smooth Muscle	stomach
20	chr5:178549600-178553600	ZNF genes & repeats	Gastric	stomach
21	chr5:178549600-178567400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr5:178550200-178556200	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr5:178550400-178565600	Weak transcription	Esophagus	oesophagus
24	chr5:178550800-178559600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:178551200-178553800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr5:178551200-178555800	Weak transcription	Fetal Muscle Leg	muscle
27	chr5:178551200-178560200	Weak transcription	Fetal Intestine Small	intestine
28	chr5:178551400-178553000	Strong transcription	NHLF	lung
29	chr5:178551400-178554400	Weak transcription	Fetal Muscle Trunk	muscle
30	chr5:178551400-178559400	Weak transcription	Fetal Lung	lung
31	chr5:178551400-178559400	Strong transcription	Osteobl	bone
32	chr5:178551600-178582800	Weak transcription	Right Atrium	heart
33	chr5:178552000-178552800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr5:178552000-178553800	ZNF genes & repeats	Lung	lung
35	chr5:178552000-178556800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
36	chr5:178552800-178553600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr5:178552800-178554200	Strong transcription	Spleen	Spleen
38	chr5:178552800-178559600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr5:178552800-178559800	Weak transcription	Right Ventricle	heart
40	chr5:178552800-178566800	Strong transcription	Fetal Stomach	stomach
41	chr5:178553000-178553800	Weak transcription	NHLF	lung
42	chr5:178553600-178553800	ZNF genes & repeats	Liver	Liver
43	chr5:178553600-178554000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr5:178553600-178556000	Weak transcription	Gastric	stomach
45	chr5:178553600-178559600	Strong transcription	Muscle Satellite Cultured Cells	--
46	chr5:178553800-178554600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:178553800-178554800	Weak transcription	Aorta	Aorta
48	chr5:178553800-178560000	Strong transcription	NHLF	lung
49	chr5:178553800-178569000	Weak transcription	Liver	Liver
50	chr5:178554000-178556600	Strong transcription	HSMMtube	muscle

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