Variant report

Variant	nsv1043967
Chromosome Location	chr9:104498664-104636328
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:664)
CpG islands
(count:429)
Chromatin interactive
region (count:19)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:104604440-104604568	K562	blood:	n/a	n/a
2	ARID3A	chr9:104603974-104604201	K562	blood:	n/a	n/a
3	ARID3A	chr9:104604790-104605089	K562	blood:	n/a	n/a
4	ARID3A	chr9:104602870-104603634	K562	blood:	n/a	n/a
5	ATF1	chr9:104602937-104603620	K562	blood:	n/a	n/a
6	ATF2	chr9:104499005-104499385	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr9:104602886-104603521	K562	blood:	n/a	n/a
8	BACH1	chr9:104500655-104501144	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr9:104603020-104603535	K562	blood:	n/a	n/a
10	BCLAF1	chr9:104602989-104603485	K562	blood:	n/a	n/a
11	BHLHE40	chr9:104602981-104603519	K562	blood:	n/a	n/a
12	BHLHE40	chr9:104629233-104629302	K562	blood:	n/a	n/a
13	BHLHE40	chr9:104603872-104603981	K562	blood:	n/a	n/a
14	BRCA1	chr9:104525751-104525924	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr9:104602902-104603580	K562	blood:	n/a	n/a
16	CBX3	chr9:104602864-104603528	K562	blood:	n/a	n/a
17	CBX3	chr9:104601296-104601594	K562	blood:	n/a	n/a
18	CCNT2	chr9:104602949-104603796	K562	blood:	n/a	n/a
19	CEBPB	chr9:104557455-104557771	Hela-S3	cervix:	n/a	chr9:104557616-104557627
20	CEBPB	chr9:104557426-104557815	K562	blood:	n/a	chr9:104557616-104557627
21	CEBPB	chr9:104520633-104520833	A549	lung:	n/a	chr9:104520734-104520745 chr9:104520733-104520744
22	CEBPB	chr9:104520587-104520900	HepG2	liver:	n/a	chr9:104520734-104520745 chr9:104520733-104520744
23	CEBPB	chr9:104557453-104557803	HepG2	liver:	n/a	chr9:104557616-104557627
24	CEBPB	chr9:104557461-104557739	H1-hESC	embryonic stem cell:	n/a	chr9:104557616-104557627
25	CEBPB	chr9:104557424-104557737	A549	lung:	n/a	chr9:104557616-104557627
26	CEBPB	chr9:104557439-104557795	IMR90	lung:	n/a	chr9:104557616-104557627
27	CEBPB	chr9:104553821-104554141	A549	lung:	n/a	n/a
28	CEBPB	chr9:104557447-104557777	A549	lung:	n/a	chr9:104557616-104557627
29	CEBPB	chr9:104571492-104571600	HepG2	liver:	n/a	chr9:104571514-104571525
30	CEBPB	chr9:104603004-104603626	K562	blood:	n/a	n/a
31	CEBPB	chr9:104602919-104603627	K562	blood:	n/a	n/a
32	CEBPB	chr9:104553838-104554309	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:104553816-104554155	IMR90	lung:	n/a	n/a
34	CEBPB	chr9:104557478-104557775	K562	blood:	n/a	chr9:104557616-104557627
35	CEBPB	chr9:104586973-104587159	HepG2	liver:	n/a	chr9:104587024-104587035 chr9:104587023-104587034 chr9:104587023-104587034
36	CEBPB	chr9:104596347-104596651	HepG2	liver:	n/a	chr9:104596523-104596534
37	CEBPB	chr9:104603213-104603499	K562	blood:	n/a	n/a
38	CEBPB	chr9:104586855-104587085	K562	blood:	n/a	chr9:104587024-104587035 chr9:104587023-104587034 chr9:104587023-104587034
39	CEBPB	chr9:104553848-104554426	K562	blood:	n/a	n/a
40	CEBPB	chr9:104557510-104557633	K562	blood:	n/a	chr9:104557616-104557627
41	CEBPB	chr9:104500497-104500505	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr9:104597034-104597167	HepG2	liver:	n/a	chr9:104597125-104597136
43	CEBPD	chr9:104602934-104603627	K562	blood:	n/a	n/a
44	CEBPD	chr9:104602898-104603672	K562	blood:	n/a	n/a
45	CHD1	chr9:104500548-104501127	H1-hESC	embryonic stem cell:	n/a	chr9:104500559-104500569
46	CHD2	chr9:104500480-104500484	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr9:104602880-104603666	K562	blood:	n/a	n/a
48	CREB1	chr9:104603097-104603501	K562	blood:	n/a	n/a
49	CTBP2	chr9:104498966-104501160	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr9:104554300-104554450	HepG2	liver:	n/a	chr9:104554408-104554426

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:104500954-104501004	HL-60	blood:	n/a
2	chr9:104500954-104501004	HMEC	breast:	n/a
3	chr9:104500954-104501004	HL-60	blood:	n/a
4	chr9:104500954-104501004	HMEC	breast:	n/a
5	chr9:104500322-104500372	MCF10A-Er-Src	breast:	n/a
6	chr9:104500958-104501008	RPTEC	kidney:	n/a
7	chr9:104500958-104501008	HRE	kidney:	n/a
8	chr9:104499700-104499750	HCF	heart:	n/a
9	chr9:104501030-104501080	BE2_C	brain:	n/a
10	chr9:104500729-104500779	HCPEpiC	choroid plexus:	n/a
11	chr9:104500954-104501004	HEEpiC	esophagus:	n/a
12	chr9:104500729-104500779	MCF10A-Er-Src	breast:	n/a
13	chr9:104499850-104499900	ECC-1	luminal epithelium:	n/a
14	chr9:104500958-104501008	BJ	skin:	n/a
15	chr9:104500958-104501008	HCF	heart:	n/a
16	chr9:104500954-104501004	HCT-116	colon:	n/a
17	chr9:104499850-104499900	NHDF-neo	bronchial:	n/a
18	chr9:104499850-104499900	CMK	blood:	n/a
19	chr9:104501030-104501080	HCPEpiC	choroid plexus:	n/a
20	chr9:104500954-104501004	HUVEC	blood vessel:	n/a
21	chr9:104501030-104501080	RPTEC	kidney:	n/a
22	chr9:104500729-104500779	A549	lung:	n/a
23	chr9:104500954-104501004	T-47D	breast:	n/a
24	chr9:104500729-104500779	AG04450	lung:	fetal
25	chr9:104500729-104500779	U87	brain:	n/a
26	chr9:104500729-104500779	HEK293	kidney:	embryo
27	chr9:104501030-104501080	HCF	heart:	n/a
28	chr9:104500954-104501004	AG09319	gingival:	n/a
29	chr9:104500954-104501004	U87	brain:	n/a
30	chr9:104499850-104499900	HRE	kidney:	n/a
31	chr9:104500729-104500779	ovcar-3	ovarian:	n/a
32	chr9:104499700-104499750	GM12891	blood:	n/a
33	chr9:104499700-104499750	GM12878	blood:	n/a
34	chr9:104501030-104501080	HRE	kidney:	n/a
35	chr9:104499700-104499750	NH-A	brain:	n/a
36	chr9:104499700-104499750	T-47D	breast:	n/a
37	chr9:104499700-104499750	BE2_C	brain:	n/a
38	chr9:104501030-104501080	HNPCEpiC	eye:	n/a
39	chr9:104499850-104499900	HRCEpiC	kidney:	n/a
40	chr9:104500954-104501004	NB4	blood:	n/a
41	chr9:104499700-104499750	IMR90	lung:	fetal
42	chr9:104499850-104499900	HEEpiC	esophagus:	n/a
43	chr9:104500729-104500779	MCF-7	breast:	n/a
44	chr9:104501030-104501080	NHBE	bronchial:	n/a
45	chr9:104500729-104500779	Hepatocyte	liver:	n/a
46	chr9:104500958-104501008	HL-60	blood:	n/a
47	chr9:104500958-104501008	NT2-D1	testis:	n/a
48	chr9:104500322-104500372	NB4	blood:	n/a
49	chr9:104500958-104501008	BE2_C	brain:	n/a
50	chr9:104500729-104500779	SK-N-SH	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:104626627..104628605-chr9:104630406..104631919,2	K562	blood:
2	chr9:104628351..104631183-chr9:104634996..104637004,2	K562	blood:
3	chr9:104628351..104631183-chr9:104634996..104637004,2	K562	blood:
4	chr9:104493214..104495968-chr9:104498085..104500159,2	K562	blood:
5	chr9:104529138..104530867-chr9:104533732..104536723,2	K562	blood:
6	chr9:104618154..104619898-chr9:104623303..104626288,2	K562	blood:
7	chr9:104602976..104605098-chr9:104654861..104656583,2	K562	blood:
8	chr9:104600370..104602657-chr9:104607856..104609607,2	K562	blood:
9	chr9:104554048..104554859-chr9:104734774..104735456,4	MCF-7	breast:
10	chr9:104534684..104536933-chr9:104538278..104540964,2	K562	blood:
11	chr9:104618154..104619898-chr9:104623303..104626288,2	K562	blood:
12	chr9:104534684..104536933-chr9:104538278..104540964,2	K562	blood:
13	chr9:104554304..104554879-chr9:107148429..107149219,2	MCF-7	breast:
14	chr9:104594444..104596154-chr9:104597009..104599073,2	MCF-7	breast:
15	chr9:104626627..104628605-chr9:104630406..104631919,2	K562	blood:
16	chr10:26587616..26588136-chr9:104616741..104617261,2	MCF-7	breast:
17	chr9:104594444..104596154-chr9:104597009..104599073,2	MCF-7	breast:
18	chr9:104600370..104602657-chr9:104607856..104609607,2	K562	blood:
19	chr9:104529138..104530867-chr9:104533732..104536723,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF20-4	chr9:104567913-104568131	NONHSAT133752
2	lnc-RNF20-4	chr9:104567769-104567808	NONHSAT133752

No data

Variant related genes	Relation type
MTND3P4	TF binding region
GRIN3A	TF binding region
MTND3P4	CpG island
GRIN3A	CpG island

Extended variants
information (count: 1690 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1690 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12340365	chr9:104498664-104498665	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562950279	chr9:104498699-104498700	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs59275233	chr9:104498730-104498731	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs59161053	chr9:104498731-104498732	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs545426742	chr9:104498733-104498734	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs200636024	chr9:104498734-104498735	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs375967078	chr9:104498761-104498762	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs564532671	chr9:104498787-104498788	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs12552239	chr9:104498788-104498789	Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs547069637	chr9:104498800-104498801	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs566986268	chr9:104498843-104498844	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs529758939	chr9:104498887-104498888	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs4474083	chr9:104498908-104498909	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs147974923	chr9:104498952-104498953	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs141647783	chr9:104498959-104498960	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs374012070	chr9:104498961-104498962	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs558925818	chr9:104498977-104498978	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs187436871	chr9:104498996-104498997	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs368006926	chr9:104499010-104499011	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs534156488	chr9:104499102-104499103	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs116117220	chr9:104499132-104499133	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs574039812	chr9:104499147-104499148	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs56236943	chr9:104499190-104499191	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs10989606	chr9:104499197-104499198	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs10989607	chr9:104499199-104499200	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs556717454	chr9:104499252-104499253	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs576603031	chr9:104499254-104499255	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs545283356	chr9:104499256-104499257	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs565267904	chr9:104499263-104499264	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs563844094	chr9:104499302-104499303	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs374026706	chr9:104499342-104499343	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs527991736	chr9:104499496-104499497	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189941998	chr9:104499498-104499499	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560721892	chr9:104499499-104499500	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370278422	chr9:104499517-104499518	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373491138	chr9:104499550-104499551	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs377410468	chr9:104499557-104499558	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368705360	chr9:104499572-104499573	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1337677	chr9:104499575-104499576	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs376812598	chr9:104499585-104499586	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368626037	chr9:104499589-104499590	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs41273935	chr9:104499617-104499618	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs532234392	chr9:104499651-104499652	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs200072366	chr9:104499677-104499678	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs182534094	chr9:104499707-104499708	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs138555829	chr9:104499725-104499726	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs372598779	chr9:104499728-104499729	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs375554113	chr9:104499737-104499738	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs142779054	chr9:104499784-104499785	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs368905495	chr9:104499847-104499848	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Neuroblastoma	20406844	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104494200-104499600	Weak transcription	Liver	Liver
2	chr9:104497800-104500000	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
3	chr9:104497800-104501200	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr9:104498600-104499600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
5	chr9:104498800-104499200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
6	chr9:104498800-104499600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
7	chr9:104499000-104499200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
8	chr9:104499000-104499400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
9	chr9:104499000-104499400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
10	chr9:104499000-104499400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
11	chr9:104499000-104499600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
12	chr9:104499000-104499600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:104499000-104499600	Bivalent/Poised TSS	Left Ventricle	heart
14	chr9:104499000-104499600	Bivalent/Poised TSS	Right Ventricle	heart
15	chr9:104499000-104500200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
16	chr9:104499000-104501200	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
17	chr9:104499200-104499400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
18	chr9:104499200-104499600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
19	chr9:104499200-104501000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
20	chr9:104499200-104501000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
21	chr9:104499400-104499600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
22	chr9:104499400-104499600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr9:104499400-104499600	Bivalent Enhancer	Brain Anterior Caudate	brain
24	chr9:104499400-104499600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
25	chr9:104499400-104499600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
26	chr9:104499400-104499600	Flanking Bivalent TSS/Enh	Fetal Heart	heart
27	chr9:104499400-104499600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
28	chr9:104499400-104500000	Enhancers	Pancreas	Pancrea
29	chr9:104499400-104500200	Bivalent Enhancer	Fetal Muscle Leg	muscle
30	chr9:104499400-104500200	Flanking Active TSS	Ovary	ovary
31	chr9:104499400-104500400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
32	chr9:104499400-104500600	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
33	chr9:104499400-104500600	Bivalent Enhancer	Fetal Brain Male	brain
34	chr9:104499400-104501000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
35	chr9:104499400-104501600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
36	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
37	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
38	chr9:104499600-104499800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
40	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
41	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
42	chr9:104499600-104499800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
43	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
44	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
45	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	Left Ventricle	heart
46	chr9:104499600-104499800	Bivalent Enhancer	Psoas Muscle	Psoas
47	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	Rectal Smooth Muscle	rectum
48	chr9:104499600-104499800	Flanking Active TSS	Right Atrium	heart
49	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
50	chr9:104499600-104500000	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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