Variant report

Variant	nsv891215
Chromosome Location	chr8:98910287-98980663
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:767)
CpG islands
(count:306)
Chromatin interactive
region (count:55)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:767 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:98930655-98930786	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:98941203-98941227	K562	blood:	n/a	n/a
3	ATF1	chr8:98944265-98944472	K562	blood:	n/a	n/a
4	ATF2	chr8:98921507-98921801	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:98945794-98945943	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:98964143-98964347	GM12878	blood:	n/a	chr8:98964231-98964241 chr8:98964230-98964241
7	BATF	chr8:98941283-98941594	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:98930844-98931020	K562	blood:	n/a	n/a
9	BHLHE40	chr8:98964147-98964347	K562	blood:	n/a	n/a
10	BHLHE40	chr8:98948265-98948433	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:98973889-98973920	K562	blood:	n/a	n/a
12	BRCA1	chr8:98934950-98934955	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr8:98920882-98921078	HepG2	liver:	n/a	chr8:98920915-98920926
14	CEBPB	chr8:98938183-98938418	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:98917394-98917742	HepG2	liver:	n/a	chr8:98917595-98917606
16	CEBPB	chr8:98942020-98942212	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:98918656-98918977	IMR90	lung:	n/a	n/a
18	CEBPB	chr8:98917409-98917735	A549	lung:	n/a	chr8:98917595-98917606
19	CEBPB	chr8:98938043-98938442	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:98964101-98964536	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr8:98920851-98920937	K562	blood:	n/a	chr8:98920915-98920926
22	CEBPB	chr8:98920881-98920910	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr8:98964128-98964593	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:98917435-98917764	A549	lung:	n/a	chr8:98917595-98917606
25	CEBPB	chr8:98920782-98921019	A549	lung:	n/a	chr8:98920915-98920926
26	CEBPB	chr8:98912506-98912665	K562	blood:	n/a	n/a
27	CEBPB	chr8:98917378-98917739	Hela-S3	cervix:	n/a	chr8:98917595-98917606
28	CEBPB	chr8:98917415-98917718	IMR90	lung:	n/a	chr8:98917595-98917606
29	CEBPB	chr8:98940864-98941573	Hela-S3	cervix:	n/a	chr8:98941081-98941094
30	CEBPB	chr8:98920845-98921058	MCF-7	breast:	n/a	chr8:98920915-98920926
31	CEBPB	chr8:98930583-98930895	IMR90	lung:	n/a	n/a
32	CEBPB	chr8:98919506-98919700	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:98965078-98965244	K562	blood:	n/a	n/a
34	CEBPB	chr8:98917415-98917637	K562	blood:	n/a	chr8:98917595-98917606
35	CHD2	chr8:98941399-98941751	GM12878	blood:	n/a	n/a
36	CHD2	chr8:98930818-98931045	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr8:98941204-98941547	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr8:98948014-98948444	GM12878	blood:	n/a	n/a
39	CHD2	chr8:98915297-98915349	HepG2	liver:	n/a	n/a
40	CTBP2	chr8:98944519-98945040	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr8:98930632-98931075	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr8:98932182-98932262	K562	blood:	n/a	n/a
43	CTCF	chr8:98930980-98931130	GM12864	blood:	n/a	n/a
44	CTCF	chr8:98937980-98938130	AG09319	gingival:	n/a	n/a
45	CTCF	chr8:98944980-98945130	BE2_C	brain:	n/a	n/a
46	CTCF	chr8:98930920-98931070	NHLF	lung:	n/a	n/a
47	CTCF	chr8:98930940-98931090	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr8:98918740-98918890	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr8:98930880-98931030	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr8:98930900-98931050	AG10803	skin:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:98944936-98944986	IMR90	lung:	fetal
2	chr8:98944936-98944986	IMR90	lung:	fetal
3	chr8:98944936-98944986	NH-A	brain:	n/a
4	chr8:98944936-98944986	HNPCEpiC	eye:	n/a
5	chr8:98963918-98963968	AG09319	gingival:	n/a
6	chr8:98963918-98963968	HCT-116	colon:	n/a
7	chr8:98956478-98956528	MCF10A-Er-Src	breast:	n/a
8	chr8:98969923-98969973	LNCaP	prostate:	n/a
9	chr8:98956478-98956528	HepG2	liver:	n/a
10	chr8:98944936-98944986	HRPEpiC	eye:	n/a
11	chr8:98956478-98956528	HCF	heart:	n/a
12	chr8:98930617-98930667	HCT-116	colon:	n/a
13	chr8:98944936-98944986	SAEC	small airway:	n/a
14	chr8:98969923-98969973	NHBE	bronchial:	n/a
15	chr8:98963918-98963968	HEEpiC	esophagus:	n/a
16	chr8:98930617-98930667	H1-hESC	embryonic stem cell:	embryo
17	chr8:98963918-98963968	GM12891	blood:	n/a
18	chr8:98963918-98963968	ECC-1	luminal epithelium:	n/a
19	chr8:98969923-98969973	HCPEpiC	choroid plexus:	n/a
20	chr8:98944936-98944986	HEEpiC	esophagus:	n/a
21	chr8:98956478-98956528	CMK	blood:	n/a
22	chr8:98963918-98963968	MCF-7	breast:	n/a
23	chr8:98930617-98930667	ECC-1	luminal epithelium:	n/a
24	chr8:98969923-98969973	Jurkat	blood:	n/a
25	chr8:98963918-98963968	ProgFib	skin:	n/a
26	chr8:98944936-98944986	Caco-2	colon:	n/a
27	chr8:98930617-98930667	Jurkat	blood:	n/a
28	chr8:98969923-98969973	SKMC	muscle:	n/a
29	chr8:98956478-98956528	AG09319	gingival:	n/a
30	chr8:98956478-98956528	BJ	skin:	n/a
31	chr8:98930617-98930667	PrEC	prostate:	n/a
32	chr8:98956478-98956528	NH-A	brain:	n/a
33	chr8:98930617-98930667	GM12891	blood:	n/a
34	chr8:98956478-98956528	HMEC	breast:	n/a
35	chr8:98956478-98956528	GM12878	blood:	n/a
36	chr8:98969923-98969973	Hepatocyte	liver:	n/a
37	chr8:98963918-98963968	NB4	blood:	n/a
38	chr8:98956478-98956528	PANC-1	pancreas:	n/a
39	chr8:98963918-98963968	Hepatocyte	liver:	n/a
40	chr8:98963918-98963968	RPTEC	kidney:	n/a
41	chr8:98930617-98930667	U87	brain:	n/a
42	chr8:98963918-98963968	A549	lung:	n/a
43	chr8:98930617-98930667	A549	lung:	n/a
44	chr8:98930617-98930667	HCF	heart:	n/a
45	chr8:98963918-98963968	HRE	kidney:	n/a
46	chr8:98944936-98944986	BE2_C	brain:	n/a
47	chr8:98930617-98930667	HRPEpiC	eye:	n/a
48	chr8:98969923-98969973	HRCEpiC	kidney:	n/a
49	chr8:98956478-98956528	AG10803	skin:	n/a
50	chr8:98969923-98969973	U87	brain:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:98933283..98934888-chr8:98936551..98939414,2	K562	blood:
2	chr17:57915257..57916823-chr8:98971519..98974188,2	MCF-7	breast:
3	chr8:98910492..98913017-chr8:98916012..98917731,2	MCF-7	breast:
4	chr8:98919725..98921829-chr8:98926428..98928167,2	MCF-7	breast:
5	chr8:98954024..98956725-chr8:98958749..98960500,2	K562	blood:
6	chr8:98941165..98944316-chr8:98945321..98948446,3	K562	blood:
7	chr8:98915826..98918784-chr8:98939816..98941350,2	MCF-7	breast:
8	chr8:98919911..98922247-chr8:99046173..99048489,2	MCF-7	breast:
9	chr8:98936307..98939164-chr8:98941664..98943484,3	K562	blood:
10	chr8:98942233..98946263-chr8:98950230..98954228,4	MCF-7	breast:
11	chr8:98964671..98967862-chr8:98969521..98972694,3	MCF-7	breast:
12	chr8:98914878..98916750-chr8:98921668..98923408,2	K562	blood:
13	chr8:98933283..98934888-chr8:98936551..98939414,2	K562	blood:
14	chr8:98966806..98971038-chr8:98972037..98974632,4	K562	blood:
15	chr8:98903943..98905489-chr8:98912302..98914031,2	MCF-7	breast:
16	chr8:98942876..98944641-chr8:98946767..98949893,3	MCF-7	breast:
17	chr8:98941087..98943572-chr8:98949558..98951176,2	K562	blood:
18	chr8:98974372..98976072-chr8:99045013..99046832,2	K562	blood:
19	chr8:98929263..98931396-chr8:99057196..99059204,2	MCF-7	breast:
20	chr8:98954807..98957086-chr8:98962023..98964271,2	MCF-7	breast:
21	chr8:98933138..98936017-chr8:98937438..98939186,2	MCF-7	breast:
22	chr8:98929481..98932017-chr8:98944998..98947169,2	MCF-7	breast:
23	chr8:98930453..98932411-chr8:98936573..98938197,2	MCF-7	breast:
24	chr8:98881106..98881826-chr8:98970641..98971277,2	MCF-7	breast:
25	chr8:98915826..98918784-chr8:98939816..98941350,2	MCF-7	breast:
26	chr8:98929481..98932017-chr8:98944998..98947169,2	MCF-7	breast:
27	chr8:98919725..98921829-chr8:98926428..98928167,2	MCF-7	breast:
28	chr8:98973467..98975670-chr8:98979919..98982620,2	MCF-7	breast:
29	chr8:98914878..98916750-chr8:98921668..98923408,2	K562	blood:
30	chr8:98964671..98967862-chr8:98969521..98972694,3	MCF-7	breast:
31	chr8:98969704..98971901-chr8:98988416..98991010,2	MCF-7	breast:
32	chr8:98961024..98963389-chr8:99054505..99057436,2	MCF-7	breast:
33	chr8:98930453..98932411-chr8:98936573..98938197,2	MCF-7	breast:
34	chr8:98933138..98936017-chr8:98937438..98939186,2	MCF-7	breast:
35	chr8:98915906..98918719-chr8:98923046..98924586,2	MCF-7	breast:
36	chr8:98917300..98918803-chr8:99024235..99026797,2	MCF-7	breast:
37	chr8:98910442..98911974-chr8:98914661..98916723,2	K562	blood:
38	chr8:98954024..98956725-chr8:98958749..98960500,2	K562	blood:
39	chr8:98940343..98943382-chr8:99056246..99058981,3	MCF-7	breast:
40	chr8:98958651..98961201-chr8:98961711..98963303,2	MCF-7	breast:
41	chr8:98910492..98913017-chr8:98916012..98917731,2	MCF-7	breast:
42	chr8:98910442..98911974-chr8:98914661..98916723,2	K562	blood:
43	chr8:98929668..98932562-chr8:98996810..98999331,2	K562	blood:
44	chr8:98949816..98952906-chr8:98954866..98958097,3	K562	blood:
45	chr8:98963788..98966015-chr8:99056664..99058893,2	MCF-7	breast:
46	chr8:98968508..98970567-chr8:98972102..98974220,2	K562	blood:
47	chr8:98905685..98907730-chr8:98945823..98947878,2	MCF-7	breast:
48	chr8:98973539..98975203-chr8:98975943..98977611,2	K562	blood:
49	chr8:98921821..98924732-chr8:98928990..98931932,2	K562	blood:
50	chr8:98915906..98918719-chr8:98923046..98924586,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LAPTM4B-4	chr8:98963047-98963126	NONHSAT127890
2	lnc-LAPTM4B-4	chr8:98964212-98964530	NONHSAT127890

No data

Variant related genes	Relation type
MATN2	TF binding region
MATN2	CpG island
ENSG00000243504	chromatin interactions
ENSG00000132561	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000156482	chromatin interactions

Extended variants
information (count: 2577 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:2577 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11996075	chr8:98910287-98910288	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74755451	chr8:98910290-98910291	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191297430	chr8:98910320-98910321	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547445166	chr8:98910381-98910382	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138939656	chr8:98910403-98910404	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573153135	chr8:98910476-98910477	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542080350	chr8:98910477-98910478	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142790231	chr8:98910541-98910542	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62521909	chr8:98910551-98910552	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183880902	chr8:98910552-98910553	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544081776	chr8:98910629-98910630	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567962839	chr8:98910635-98910636	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs367938947	chr8:98910680-98910681	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373035269	chr8:98910725-98910726	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545774723	chr8:98910726-98910727	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371928106	chr8:98910750-98910751	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559348124	chr8:98910751-98910752	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188496749	chr8:98910757-98910758	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181310700	chr8:98910782-98910783	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185046199	chr8:98910802-98910803	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531086783	chr8:98910829-98910830	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs147408672	chr8:98910861-98910862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556338623	chr8:98910863-98910864	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570551094	chr8:98910883-98910884	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189976913	chr8:98910885-98910886	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72675237	chr8:98910894-98910895	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs558733259	chr8:98910907-98910908	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538834246	chr8:98910928-98910929	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566442333	chr8:98910982-98910983	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370228310	chr8:98910998-98910999	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs13265992	chr8:98911007-98911008	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs13268171	chr8:98911008-98911009	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535117485	chr8:98911039-98911040	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557866107	chr8:98911040-98911041	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114455602	chr8:98911062-98911063	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561698847	chr8:98911083-98911084	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538037930	chr8:98911113-98911114	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375940737	chr8:98911124-98911125	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs62521910	chr8:98911143-98911144	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs63493662	chr8:98911153-98911154	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576903147	chr8:98911189-98911190	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545861142	chr8:98911204-98911205	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559433255	chr8:98911271-98911272	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182088217	chr8:98911280-98911281	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559854661	chr8:98911315-98911316	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111806187	chr8:98911363-98911364	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562401412	chr8:98911365-98911366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531149126	chr8:98911382-98911383	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371238049	chr8:98911431-98911432	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551175296	chr8:98911443-98911444	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Malignant melanoma	17260012	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Intellectual disability	21811512	CNVD

Chromatin state (count:1759 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:98882400-98914800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:98884200-98915000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr8:98884200-98915000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr8:98892000-98915200	Weak transcription	Colonic Mucosa	Colon
5	chr8:98892000-98918800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr8:98893400-98912000	Weak transcription	Fetal Intestine Small	intestine
7	chr8:98894000-98918600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr8:98898800-98917600	Weak transcription	Adipose Nuclei	Adipose
9	chr8:98899800-98915000	Weak transcription	Liver	Liver
10	chr8:98900400-98914400	Weak transcription	Pancreas	Pancrea
11	chr8:98900600-98911200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:98901000-98913600	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr8:98901000-98913800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr8:98903400-98918200	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr8:98903600-98912400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:98903600-98918400	Weak transcription	Brain Substantia Nigra	brain
17	chr8:98903600-98924200	Weak transcription	Fetal Kidney	kidney
18	chr8:98904000-98927600	Weak transcription	Esophagus	oesophagus
19	chr8:98905400-98918400	Weak transcription	Brain Hippocampus Middle	brain
20	chr8:98907200-98910600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:98907800-98915000	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr8:98908800-98910600	Enhancers	Fetal Lung	lung
23	chr8:98908800-98910600	Enhancers	NHLF	lung
24	chr8:98908800-98912000	Enhancers	Fetal Stomach	stomach
25	chr8:98909200-98913800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:98909200-98916200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr8:98909400-98910400	Enhancers	Osteobl	bone
28	chr8:98909400-98913400	Strong transcription	Fetal Muscle Trunk	muscle
29	chr8:98909400-98915000	Weak transcription	Duodenum Mucosa	Duodenum
30	chr8:98909800-98910400	Weak transcription	Ovary	ovary
31	chr8:98909800-98913200	Strong transcription	Fetal Muscle Leg	muscle
32	chr8:98910000-98910600	Enhancers	Placenta	Placenta
33	chr8:98910000-98921200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr8:98910200-98910400	Enhancers	A549	lung
35	chr8:98910200-98912000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:98910200-98912400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr8:98910400-98910600	Enhancers	Ovary	ovary
38	chr8:98910400-98912000	Weak transcription	Osteobl	bone
39	chr8:98910600-98911800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr8:98910600-98911800	Weak transcription	Placenta	Placenta
41	chr8:98910600-98912000	Weak transcription	Ovary	ovary
42	chr8:98910600-98913600	Weak transcription	Fetal Lung	lung
43	chr8:98911800-98912400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr8:98911800-98913400	Enhancers	Placenta	Placenta
45	chr8:98912000-98912800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:98912000-98912800	Strong transcription	Fetal Intestine Small	intestine
47	chr8:98912000-98912800	Genic enhancers	Fetal Stomach	stomach
48	chr8:98912000-98912800	Enhancers	Osteobl	bone
49	chr8:98912000-98913600	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr8:98912000-98916000	Strong transcription	Ovary	ovary

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