Variant report

Variant	nsv1023409
Chromosome Location	chr8:48320442-48454089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1365)
CpG islands
(count:733)
Chromatin interactive
region (count:67)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1365 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48437168-48437824	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:48425108-48425339	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:48370977-48371215	K562	blood:	n/a	n/a
4	ARID3A	chr8:48352874-48353560	K562	blood:	n/a	chr8:48353449-48353465
5	ARID3A	chr8:48385021-48385529	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:48371417-48371596	K562	blood:	n/a	n/a
7	ARID3A	chr8:48371879-48372001	K562	blood:	n/a	n/a
8	ATF1	chr8:48370999-48371277	K562	blood:	n/a	n/a
9	ATF1	chr8:48353062-48353371	K562	blood:	n/a	n/a
10	ATF1	chr8:48444199-48444363	K562	blood:	n/a	n/a
11	ATF2	chr8:48351488-48352019	GM12878	blood:	n/a	n/a
12	ATF2	chr8:48351620-48351896	GM12878	blood:	n/a	n/a
13	ATF2	chr8:48426073-48426690	GM12878	blood:	n/a	n/a
14	ATF2	chr8:48424919-48425438	H1-hESC	embryonic stem cell:	n/a	chr8:48425190-48425201
15	ATF2	chr8:48424960-48425389	H1-hESC	embryonic stem cell:	n/a	chr8:48425190-48425201
16	ATF2	chr8:48426005-48426751	GM12878	blood:	n/a	n/a
17	ATF3	chr8:48424988-48425460	A549	lung:	n/a	chr8:48425192-48425202 chr8:48425189-48425202 chr8:48425192-48425199 chr8:48425188-48425203 chr8:48425189-48425199 chr8:48425190-48425201 chr8:48425192-48425200 chr8:48425188-48425201 chr8:48425189-48425199 chr8:48425189-48425202 chr8:48425192-48425202 chr8:48425190-48425201 chr8:48425190-48425203 chr8:48425189-48425200
18	ATF3	chr8:48424961-48425457	A549	lung:	n/a	chr8:48425192-48425202 chr8:48425189-48425202 chr8:48425192-48425199 chr8:48425188-48425203 chr8:48425189-48425199 chr8:48425190-48425201 chr8:48425192-48425200 chr8:48425188-48425201 chr8:48425189-48425199 chr8:48425189-48425202 chr8:48425192-48425202 chr8:48425190-48425201 chr8:48425190-48425203 chr8:48425189-48425200
19	ATF3	chr8:48343852-48344341	K562	blood:	n/a	n/a
20	BACH1	chr8:48344301-48344555	K562	blood:	n/a	n/a
21	BACH1	chr8:48426078-48426349	K562	blood:	n/a	chr8:48426195-48426209
22	BACH1	chr8:48425999-48426602	H1-hESC	embryonic stem cell:	n/a	chr8:48426195-48426209
23	BATF	chr8:48426050-48426304	GM12878	blood:	n/a	chr8:48426194-48426205 chr8:48426195-48426205
24	BATF	chr8:48351608-48351855	GM12878	blood:	n/a	n/a
25	BATF	chr8:48420269-48420728	GM12878	blood:	n/a	n/a
26	BATF	chr8:48426321-48426864	GM12878	blood:	n/a	n/a
27	BATF	chr8:48351639-48351872	GM12878	blood:	n/a	n/a
28	BATF	chr8:48426328-48426884	GM12878	blood:	n/a	n/a
29	BCL3	chr8:48424834-48425773	A549	lung:	n/a	chr8:48425167-48425176
30	BCL3	chr8:48422245-48422583	GM12878	blood:	n/a	n/a
31	BCL3	chr8:48424904-48425461	A549	lung:	n/a	chr8:48425167-48425176
32	BCL3	chr8:48438582-48439175	A549	lung:	n/a	n/a
33	BCL3	chr8:48437371-48437990	A549	lung:	n/a	n/a
34	BCL3	chr8:48437323-48438105	A549	lung:	n/a	n/a
35	BCL3	chr8:48425843-48426604	A549	lung:	n/a	n/a
36	BHLHE40	chr8:48392120-48392554	K562	blood:	n/a	n/a
37	BHLHE40	chr8:48343922-48344285	K562	blood:	n/a	n/a
38	BHLHE40	chr8:48426233-48426728	GM12878	blood:	n/a	n/a
39	BHLHE40	chr8:48421174-48421309	GM12878	blood:	n/a	n/a
40	BRCA1	chr8:48425001-48425515	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr8:48425996-48426067	H1-hESC	embryonic stem cell:	n/a	n/a
42	CBX3	chr8:48333368-48333683	K562	blood:	n/a	n/a
43	CBX3	chr8:48352960-48353333	K562	blood:	n/a	n/a
44	CBX3	chr8:48333378-48333582	K562	blood:	n/a	n/a
45	CBX3	chr8:48425865-48426825	HCT-116	colon:	n/a	chr8:48426116-48426127
46	CBX3	chr8:48343909-48344313	K562	blood:	n/a	n/a
47	CBX3	chr8:48352862-48353396	K562	blood:	n/a	n/a
48	CBX3	chr8:48366223-48366540	K562	blood:	n/a	n/a
49	CEBPB	chr8:48388750-48389296	HCT-116	colon:	n/a	n/a
50	CEBPB	chr8:48411299-48411667	A549	lung:	n/a	chr8:48411483-48411496

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48394027-48394077	AG04450	lung:	fetal
2	chr8:48394027-48394077	AG04450	lung:	fetal
3	chr8:48389903-48389953	LNCaP	prostate:	n/a
4	chr8:48389903-48389953	U87	brain:	n/a
5	chr8:48343009-48343059	GM12878	blood:	n/a
6	chr8:48427018-48427068	GM06990	blood:	n/a
7	chr8:48385636-48385686	NT2-D1	testis:	n/a
8	chr8:48418220-48418270	GM19239	blood:	n/a
9	chr8:48418220-48418270	NB4	blood:	n/a
10	chr8:48343009-48343059	MCF-7	breast:	n/a
11	chr8:48389903-48389953	Hela-S3	cervix:	n/a
12	chr8:48325740-48325790	LNCaP	prostate:	n/a
13	chr8:48385636-48385686	HIPEpiC	eye:	n/a
14	chr8:48418189-48418239	HCM	heart:	n/a
15	chr8:48352024-48352074	H1-hESC	embryonic stem cell:	embryo
16	chr8:48325740-48325790	AG04450	lung:	fetal
17	chr8:48418220-48418270	ECC-1	luminal epithelium:	n/a
18	chr8:48389903-48389953	BE2_C	brain:	n/a
19	chr8:48418189-48418239	A549	lung:	n/a
20	chr8:48389903-48389953	HMEC	breast:	n/a
21	chr8:48344060-48344110	ProgFib	skin:	n/a
22	chr8:48389903-48389953	HL-60	blood:	n/a
23	chr8:48389903-48389953	GM12878	blood:	n/a
24	chr8:48397680-48397730	HEK293	kidney:	embryo
25	chr8:48352024-48352074	SAEC	small airway:	n/a
26	chr8:48389903-48389953	NHDF-neo	bronchial:	n/a
27	chr8:48418189-48418239	AG04449	skin:	fetal
28	chr8:48352024-48352074	NT2-D1	testis:	n/a
29	chr8:48437852-48437902	AG10803	skin:	n/a
30	chr8:48352024-48352074	Jurkat	blood:	n/a
31	chr8:48397680-48397730	NHDF-neo	bronchial:	n/a
32	chr8:48418220-48418270	HepG2	liver:	n/a
33	chr8:48325740-48325790	GM12892	blood:	n/a
34	chr8:48343009-48343059	HMEC	breast:	n/a
35	chr8:48394027-48394077	SK-N-MC	brain:	n/a
36	chr8:48418189-48418239	SAEC	small airway:	n/a
37	chr8:48325740-48325790	MCF10A-Er-Src	breast:	n/a
38	chr8:48437852-48437902	NT2-D1	testis:	n/a
39	chr8:48437852-48437902	T-47D	breast:	n/a
40	chr8:48344060-48344110	IMR90	lung:	fetal
41	chr8:48427018-48427068	GM12891	blood:	n/a
42	chr8:48343009-48343059	HepG2	liver:	n/a
43	chr8:48385636-48385686	BJ	skin:	n/a
44	chr8:48427018-48427068	HCM	heart:	n/a
45	chr8:48343009-48343059	NB4	blood:	n/a
46	chr8:48385636-48385686	ProgFib	skin:	n/a
47	chr8:48394027-48394077	MCF-7	breast:	n/a
48	chr8:48394027-48394077	HCPEpiC	choroid plexus:	n/a
49	chr8:48344060-48344110	NB4	blood:	n/a
50	chr8:48394027-48394077	HEK293	kidney:	embryo

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:48431010..48432979-chr8:48435160..48436961,2	K562	blood:
2	chr8:48425055..48429090-chr8:48432986..48438786,8	MCF-7	breast:
3	chr8:48355119..48356977-chr8:48650135..48651747,2	MCF-7	breast:
4	chr8:48420026..48420889-chr8:48651231..48651938,2	MCF-7	breast:
5	chr8:48385290..48387573-chr8:48390610..48393491,2	K562	blood:
6	chr8:48367371..48370360-chr8:48387599..48389529,2	MCF-7	breast:
7	chr8:48421398..48423203-chr8:48423816..48426679,2	K562	blood:
8	chr8:48424864..48427564-chr8:48437009..48439123,4	MCF-7	breast:
9	chr8:48430927..48433174-chr8:48436968..48438708,2	K562	blood:
10	chr8:48425858..48428805-chr8:48433583..48436429,2	MCF-7	breast:
11	chr6:58777113..58777667-chr8:48324823..48325324,2	MCF-7	breast:
12	chr8:48391175..48393987-chr8:48395475..48396988,2	K562	blood:
13	chr8:48353630..48357760-chr8:48647568..48650478,4	MCF-7	breast:
14	chr8:48403369..48405723-chr8:48406802..48408473,2	K562	blood:
15	chr8:48433892..48441630-chr8:48644198..48652247,18	MCF-7	breast:
16	chr8:48430923..48433623-chr8:48450374..48452837,2	MCF-7	breast:
17	chr8:48424864..48427564-chr8:48437009..48439123,4	MCF-7	breast:
18	chr8:48356855..48359120-chr8:48360293..48362250,2	K562	blood:
19	chr8:48320531..48322399-chr8:48323544..48325394,2	MCF-7	breast:
20	chr8:48391175..48393987-chr8:48395475..48396988,2	K562	blood:
21	chr8:48435895..48437509-chr8:48455733..48457442,2	MCF-7	breast:
22	chr8:48435448..48437603-chr8:48438806..48441568,2	K562	blood:
23	chr8:48428692..48431572-chr8:48649357..48651752,3	MCF-7	breast:
24	chr8:48337815..48339899-chr8:48341496..48344035,2	MCF-7	breast:
25	chr8:48453211..48456325-chr8:48648153..48651831,4	MCF-7	breast:
26	chr8:48326655..48329493-chr8:48335487..48337638,2	K562	blood:
27	chr8:48404469..48406419-chr8:48408750..48411124,2	K562	blood:
28	chr8:48418430..48420641-chr8:48424490..48426967,2	K562	blood:
29	chr8:48342172..48345072-chr8:48346372..48349504,3	K562	blood:
30	chr8:48320531..48322399-chr8:48323544..48325394,2	MCF-7	breast:
31	chr8:48342172..48345072-chr8:48346372..48349504,3	K562	blood:
32	chr8:48404469..48406419-chr8:48408750..48411124,2	K562	blood:
33	chr8:48345796..48347342-chr8:48349198..48352084,2	MCF-7	breast:
34	chr8:48435225..48441849-chr8:48646333..48652657,17	MCF-7	breast:
35	chr8:48425055..48429090-chr8:48432986..48438786,8	MCF-7	breast:
36	chr8:48441687..48444204-chr8:48648313..48651863,3	MCF-7	breast:
37	chr8:48352837..48354610-chr8:48358749..48360682,2	K562	blood:
38	chr8:48338641..48341078-chr8:48342654..48345157,3	K562	blood:
39	chr8:48345864..48348499-chr8:48349086..48353866,5	K562	blood:
40	chr8:48316678..48319260-chr8:48343262..48344870,2	MCF-7	breast:
41	chr8:48333919..48335509-chr8:48339722..48341416,2	K562	blood:
42	chr8:48417465..48419958-chr8:48587324..48588844,2	MCF-7	breast:
43	chr8:48337815..48339899-chr8:48341496..48344035,2	MCF-7	breast:
44	chr8:48403369..48405723-chr8:48406802..48408473,2	K562	blood:
45	chr8:48424729..48427909-chr8:48454789..48458165,3	MCF-7	breast:
46	chr8:48343800..48344570-chr8:48513956..48514755,2	MCF-7	breast:
47	chr8:48326655..48329493-chr8:48335487..48337638,2	K562	blood:
48	chr8:48367371..48370360-chr8:48387599..48389529,2	MCF-7	breast:
49	chr6:58776812..58777737-chr8:48324823..48325324,2	MCF-7	breast:
50	chr8:48432437..48435065-chr8:48648132..48650719,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1134I14.8.1-7	chr8:48439959-48440710	ENSG00000269924.1

No data

Variant related genes	Relation type
ENSG00000253330	TF binding region
ENSG00000269924	TF binding region
SPIDR	TF binding region
ENSG00000253330	CpG island
ENSG00000269924	CpG island
SPIDR	CpG island
ENSG00000221869	chromatin interactions
ENSG00000253330	chromatin interactions
ENSG00000164808	chromatin interactions
ENSG00000269924	chromatin interactions

Extended variants
information (count: 4986 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:4986 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556176961	chr8:48320455-48320456	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182613962	chr8:48320461-48320462	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373712077	chr8:48320469-48320470	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377425115	chr8:48320495-48320496	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535412315	chr8:48320509-48320510	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs17612211	chr8:48320529-48320530	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112059332	chr8:48320564-48320565	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193295045	chr8:48320567-48320568	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546398027	chr8:48320598-48320599	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141513742	chr8:48320627-48320628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564508678	chr8:48320631-48320632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35350751	chr8:48320670-48320671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371467598	chr8:48320674-48320675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558058320	chr8:48320752-48320753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576850861	chr8:48320772-48320773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544125109	chr8:48320780-48320781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562323025	chr8:48320785-48320786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529726171	chr8:48320789-48320790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547845082	chr8:48320808-48320809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144591368	chr8:48320831-48320832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527376487	chr8:48320897-48320898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs578017134	chr8:48320906-48320907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552381297	chr8:48320919-48320920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570301566	chr8:48320977-48320978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537792272	chr8:48321001-48321002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543698968	chr8:48321032-48321033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9657080	chr8:48321047-48321048	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs375447574	chr8:48321080-48321081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535471738	chr8:48321093-48321094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536368685	chr8:48321095-48321096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553851077	chr8:48321106-48321107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572528631	chr8:48321127-48321128	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185544434	chr8:48321176-48321177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138550865	chr8:48321220-48321221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576714815	chr8:48321234-48321235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200355604	chr8:48321244-48321245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543993516	chr8:48321248-48321249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35364680	chr8:48321279-48321280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562385762	chr8:48321334-48321335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574362403	chr8:48321396-48321397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541839451	chr8:48321465-48321466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141198315	chr8:48321476-48321477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557528152	chr8:48321484-48321485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527420791	chr8:48321488-48321489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551981064	chr8:48321504-48321505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187480323	chr8:48321507-48321508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576061329	chr8:48321545-48321546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192040131	chr8:48321546-48321547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574303050	chr8:48321553-48321554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543328806	chr8:48321562-48321563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:2779 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48282400-48321200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr8:48290800-48322200	Weak transcription	Liver	Liver
3	chr8:48290800-48347400	Weak transcription	HepG2	liver
4	chr8:48295800-48324400	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr8:48298200-48325600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr8:48298400-48325400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr8:48298600-48325600	Weak transcription	Osteobl	bone
8	chr8:48299600-48331600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr8:48300400-48331400	Weak transcription	Fetal Brain Male	brain
10	chr8:48300800-48325600	Weak transcription	HMEC	breast
11	chr8:48301400-48341200	Weak transcription	HSMMtube	muscle
12	chr8:48301600-48325600	Weak transcription	Adipose Nuclei	Adipose
13	chr8:48303800-48328000	Weak transcription	Ovary	ovary
14	chr8:48307400-48328000	Weak transcription	GM12878-XiMat	blood
15	chr8:48308400-48343600	Weak transcription	Colonic Mucosa	Colon
16	chr8:48308600-48322600	Weak transcription	HUVEC	blood vessel
17	chr8:48308600-48328000	Weak transcription	HSMM	muscle
18	chr8:48308800-48322000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr8:48308800-48331000	Weak transcription	Brain Hippocampus Middle	brain
20	chr8:48308800-48341200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr8:48310000-48350600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr8:48310400-48320800	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr8:48310400-48327800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr8:48310600-48325600	Weak transcription	NHEK	skin
25	chr8:48310600-48343600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr8:48310800-48354800	Weak transcription	Right Ventricle	heart
27	chr8:48311600-48353000	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr8:48311800-48329800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr8:48312000-48328000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr8:48312000-48328000	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr8:48312000-48349000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr8:48312200-48322200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:48312200-48353000	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr8:48312400-48341200	Weak transcription	K562	blood
35	chr8:48312600-48320800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr8:48312800-48320800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr8:48312800-48322200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr8:48312800-48322200	Weak transcription	Spleen	Spleen
39	chr8:48312800-48325400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr8:48312800-48325600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr8:48312800-48325600	Weak transcription	Gastric	stomach
42	chr8:48312800-48325600	Weak transcription	Lung	lung
43	chr8:48312800-48327800	Weak transcription	Fetal Muscle Trunk	muscle
44	chr8:48312800-48328000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr8:48312800-48342600	Weak transcription	Left Ventricle	heart
46	chr8:48312800-48342600	Weak transcription	Stomach Smooth Muscle	stomach
47	chr8:48312800-48358600	Weak transcription	Thymus	Thymus
48	chr8:48312800-48367600	Weak transcription	Pancreas	Pancrea
49	chr8:48312800-48377000	Weak transcription	Esophagus	oesophagus
50	chr8:48313000-48322200	Weak transcription	Fetal Stomach	stomach

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