Variant report

Variant	esv3326686
Chromosome Location	chr9:140483956-140486504
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:543)
CpG islands
(count:306)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:140485031-140485339	K562	blood:	n/a	n/a
2	BACH1	chr9:140485179-140485711	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr9:140484981-140485173	GM12878	blood:	n/a	chr9:140484994-140485010
4	BHLHE40	chr9:140485106-140485787	K562	blood:	n/a	n/a
5	BHLHE40	chr9:140484293-140484320	K562	blood:	n/a	n/a
6	BRCA1	chr9:140485061-140485374	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr9:140485669-140485806	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr9:140484074-140484402	K562	blood:	n/a	n/a
9	CBX3	chr9:140485008-140485350	K562	blood:	n/a	n/a
10	CBX3	chr9:140485475-140485908	K562	blood:	n/a	n/a
11	CCNT2	chr9:140484363-140485671	K562	blood:	n/a	chr9:140484967-140484976
12	CEBPB	chr9:140485019-140485299	Hela-S3	cervix:	n/a	n/a
13	CHD1	chr9:140484691-140484798	GM12878	blood:	n/a	n/a
14	CHD1	chr9:140484266-140484413	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr9:140485289-140485515	H1-hESC	embryonic stem cell:	n/a	chr9:140485385-140485395 chr9:140485374-140485384
16	CHD1	chr9:140483939-140485824	IMR90	lung:	n/a	chr9:140485385-140485395 chr9:140485374-140485384 chr9:140484887-140484897 chr9:140484968-140484978
17	CHD2	chr9:140485060-140485300	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr9:140485050-140485332	HepG2	liver:	n/a	n/a
19	CHD2	chr9:140484968-140485353	K562	blood:	n/a	chr9:140484968-140484978
20	CHD2	chr9:140484834-140485736	Hela-S3	cervix:	n/a	chr9:140485385-140485395 chr9:140485374-140485384 chr9:140484887-140484897 chr9:140484968-140484978
21	CHD2	chr9:140484971-140485429	GM12878	blood:	n/a	chr9:140485385-140485395 chr9:140485374-140485384
22	CREB1	chr9:140484891-140485740	HepG2	liver:	n/a	n/a
23	CREB1	chr9:140484857-140485561	GM12878	blood:	n/a	n/a
24	CREB1	chr9:140484909-140485464	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr9:140484896-140485575	K562	blood:	n/a	n/a
26	CREB1	chr9:140485000-140485389	ECC-1	luminal epithelium:	n/a	n/a
27	CREB1	chr9:140484907-140485442	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr9:140484706-140485587	A549	lung:	n/a	n/a
29	CREB1	chr9:140485027-140485434	ECC-1	luminal epithelium:	n/a	n/a
30	CREB1	chr9:140484990-140485312	A549	lung:	n/a	n/a
31	CREB1	chr9:140484736-140485640	HepG2	liver:	n/a	n/a
32	CREB1	chr9:140483817-140484116	A549	lung:	n/a	n/a
33	CREB1	chr9:140484914-140485505	K562	blood:	n/a	n/a
34	CTCF	chr9:140485200-140485350	HepG2	liver:	n/a	n/a
35	CTCF	chr9:140485560-140485710	GM12870	blood:	n/a	n/a
36	CTCF	chr9:140485200-140485350	BJ	skin:	n/a	n/a
37	CTCF	chr9:140485680-140485830	RPTEC	kidney:	n/a	n/a
38	CTCF	chr9:140485620-140485770	AG04449	skin:	n/a	n/a
39	CTCF	chr9:140484252-140484309	GM10248	blood:	n/a	n/a
40	CTCF	chr9:140485140-140485290	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr9:140485222-140485230	GM19238	blood:	n/a	n/a
42	CTCF	chr9:140485662-140485818	K562	blood:	n/a	n/a
43	CTCF	chr9:140485640-140485790	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr9:140485680-140485830	SAEC	small airway:	n/a	n/a
45	CTCF	chr9:140485169-140485215	GM19238	blood:	n/a	n/a
46	CTCF	chr9:140485652-140485809	MCF-7	breast:	n/a	n/a
47	CTCF	chr9:140485620-140485770	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr9:140485640-140485790	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr9:140485640-140485790	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr9:140485706-140485759	H1-hESC	embryonic stem cell:	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	chr9:140485596-140485646	K562	blood:	n/a
2	chr9:140485596-140485646	K562	blood:	n/a
3	chr9:140485596-140485646	Hepatocyte	liver:	n/a
4	chr9:140484847-140484897	NB4	blood:	n/a
5	chr9:140484220-140484270	AG09319	gingival:	n/a
6	chr9:140484977-140485027	GM06990	blood:	n/a
7	chr9:140485596-140485646	HAEpiC	amniotic membrane:	n/a
8	chr9:140484847-140484897	U87	brain:	n/a
9	chr9:140484847-140484897	SK-N-SH_RA	brain:	n/a
10	chr9:140485720-140485770	AoSMC	blood vessel:	n/a
11	chr9:140484977-140485027	HUVEC	blood vessel:	n/a
12	chr9:140485596-140485646	NHDF-neo	bronchial:	n/a
13	chr9:140484847-140484897	SK-N-SH	brain:	n/a
14	chr9:140484847-140484897	ECC-1	luminal epithelium:	n/a
15	chr9:140484977-140485027	HRCEpiC	kidney:	n/a
16	chr9:140484220-140484270	U87	brain:	n/a
17	chr9:140485596-140485646	HCPEpiC	choroid plexus:	n/a
18	chr9:140485596-140485646	SAEC	small airway:	n/a
19	chr9:140485596-140485646	HL-60	blood:	n/a
20	chr9:140484977-140485027	PANC-1	pancreas:	n/a
21	chr9:140485720-140485770	AG04450	lung:	fetal
22	chr9:140484220-140484270	Caco-2	colon:	n/a
23	chr9:140485596-140485646	NHBE	bronchial:	n/a
24	chr9:140484977-140485027	SK-N-SH_RA	brain:	n/a
25	chr9:140484847-140484897	SKMC	muscle:	n/a
26	chr9:140484977-140485027	H1-hESC	embryonic stem cell:	embryo
27	chr9:140485596-140485646	SK-N-MC	brain:	n/a
28	chr9:140484847-140484897	RPTEC	kidney:	n/a
29	chr9:140484847-140484897	HRPEpiC	eye:	n/a
30	chr9:140484220-140484270	GM12892	blood:	n/a
31	chr9:140484220-140484270	SAEC	small airway:	n/a
32	chr9:140484220-140484270	AoSMC	blood vessel:	n/a
33	chr9:140484220-140484270	Hepatocyte	liver:	n/a
34	chr9:140485596-140485646	AG09309	skin:	n/a
35	chr9:140484847-140484897	SK-N-MC	brain:	n/a
36	chr9:140484847-140484897	HEEpiC	esophagus:	n/a
37	chr9:140484977-140485027	HCPEpiC	choroid plexus:	n/a
38	chr9:140485596-140485646	A549	lung:	n/a
39	chr9:140484847-140484897	NT2-D1	testis:	n/a
40	chr9:140484220-140484270	NHDF-neo	bronchial:	n/a
41	chr9:140485596-140485646	Caco-2	colon:	n/a
42	chr9:140485596-140485646	HEEpiC	esophagus:	n/a
43	chr9:140484847-140484897	AG09309	skin:	n/a
44	chr9:140484977-140485027	HPAEpiC	pulmonary alveolar:	n/a
45	chr9:140484220-140484270	ovcar-3	ovarian:	n/a
46	chr9:140484847-140484897	AoSMC	blood vessel:	n/a
47	chr9:140484977-140485027	HAEpiC	amniotic membrane:	n/a
48	chr9:140484847-140484897	HepG2	liver:	n/a
49	chr9:140485720-140485770	LNCaP	prostate:	n/a
50	chr9:140484220-140484270	BE2_C	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:140480405..140490432-chr9:140494944..140502746,26	K562	blood:
2	chr9:140482399..140489274-chr9:140503366..140510626,23	MCF-7	breast:
3	chr10:74033371..74034211-chr9:140484641..140485198,2	Hela-S3	cervix:
4	chr9:140481402..140486615-chr9:140511490..140514947,5	K562	blood:
5	chr9:140482066..140484246-chr9:140508462..140511181,2	K562	blood:
6	chr9:140443475..140446294-chr9:140484220..140486836,3	MCF-7	breast:
7	chr9:140482416..140489757-chr9:140495738..140502746,21	K562	blood:
8	chr9:140484029..140484784-chr9:140499884..140500416,2	MCF-7	breast:
9	chr14:67826020..67826820-chr9:140484636..140485558,2	Hela-S3	cervix:
10	chr9:128002978..128003976-chr9:140484864..140485791,2	Hela-S3	cervix:
11	chr9:140481390..140486340-chr9:140509681..140515296,7	K562	blood:
12	chr9:140482616..140489091-chr9:140495925..140503345,17	MCF-7	breast:
13	chr9:140485234..140487017-chr9:140490927..140493336,2	MCF-7	breast:
14	chr22:30238285..30239003-chr9:140485780..140486690,2	MCF-7	breast:
15	chr9:140470526..140476841-chr9:140479974..140487037,14	MCF-7	breast:
16	chr9:140481624..140488545-chr9:140511605..140516057,16	MCF-7	breast:
17	chr9:140485611..140487134-chr9:140558504..140560713,2	MCF-7	breast:
18	chr9:140483300..140485633-chr9:140485903..140489005,3	MCF-7	breast:

No data

Variant related genes	Relation type
ZMYND19	TF binding region
ZMYND19	CpG island
ENSG00000148399	chromatin interactions
ENSG00000168209	chromatin interactions
ENSG00000134001	chromatin interactions
ENSG00000239705	chromatin interactions
ENSG00000181090	chromatin interactions
ENSG00000197070	chromatin interactions
ENSG00000165724	chromatin interactions
ENSG00000100554	chromatin interactions
ENSG00000203993	chromatin interactions
ENSG00000130653	chromatin interactions
ENSG00000182154	chromatin interactions
ENSG00000044574	chromatin interactions

Extended variants
information (count: 82 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553162910	chr9:140483977-140483978	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs150890156	chr9:140483982-140483983	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs573065792	chr9:140484035-140484036	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs538784711	chr9:140484046-140484047	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs370573611	chr9:140484061-140484062	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs114222989	chr9:140484065-140484066	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs575565909	chr9:140484100-140484101	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs544568348	chr9:140484114-140484115	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs115062061	chr9:140484133-140484134	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs574754159	chr9:140484195-140484196	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs540517923	chr9:140484234-140484235	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs191714020	chr9:140484255-140484256	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs145142141	chr9:140484256-140484257	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs532721401	chr9:140484339-140484340	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs551224772	chr9:140484374-140484375	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs564961087	chr9:140484401-140484402	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs530446752	chr9:140484421-140484422	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs550549762	chr9:140484436-140484437	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs567577151	chr9:140484440-140484441	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs565073797	chr9:140484459-140484460	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs536591259	chr9:140484494-140484495	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs2353078	chr9:140484517-140484518	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs12344960	chr9:140484530-140484531	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs564579895	chr9:140484597-140484598	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs140320057	chr9:140484641-140484642	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	mRNA abundance
26	rs538792196	chr9:140484649-140484650	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs558804846	chr9:140484785-140484786	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs183541102	chr9:140484825-140484826	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs537859239	chr9:140484826-140484827	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs554582475	chr9:140484841-140484842	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs574486640	chr9:140484966-140484967	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
32	rs540550377	chr9:140485038-140485039	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs554030867	chr9:140485044-140485045	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs149675488	chr9:140485116-140485117	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
35	rs546352807	chr9:140485172-140485173	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs564834290	chr9:140485208-140485209	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs530587809	chr9:140485211-140485212	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs550845800	chr9:140485233-140485234	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs187099792	chr9:140485306-140485307	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs112490360	chr9:140485317-140485318	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs529698775	chr9:140485324-140485325	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs12685070	chr9:140485341-140485342	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs546931856	chr9:140485344-140485345	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs566729838	chr9:140485359-140485360	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs564485747	chr9:140485373-140485374	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs112420688	chr9:140485437-140485438	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs112591423	chr9:140485499-140485500	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs560889174	chr9:140485502-140485503	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs532208170	chr9:140485509-140485510	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs552307445	chr9:140485510-140485511	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:20)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:465 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140482200-140484200	Weak transcription	Aorta	Aorta
2	chr9:140482600-140484400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:140482800-140484000	Enhancers	Left Ventricle	heart
4	chr9:140482800-140484000	Transcr. at gene 5' and 3'	Dnd41	blood
5	chr9:140483000-140484000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:140483000-140484200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:140483000-140484200	Flanking Active TSS	GM12878-XiMat	blood
8	chr9:140483200-140484000	Flanking Active TSS	NHDF-Ad	bronchial
9	chr9:140483200-140484200	Enhancers	Stomach Mucosa	stomach
10	chr9:140483400-140484000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr9:140483400-140484000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:140483400-140484000	Enhancers	Primary B cells from cord blood	blood
13	chr9:140483400-140484000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr9:140483400-140484000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
15	chr9:140483400-140484000	Enhancers	Fetal Lung	lung
16	chr9:140483400-140484000	Enhancers	Placenta Amnion	Placenta Amnion
17	chr9:140483400-140484000	Flanking Active TSS	HepG2	liver
18	chr9:140483400-140484200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
19	chr9:140483400-140484200	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
20	chr9:140483400-140484200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr9:140483400-140484200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr9:140483400-140484200	Enhancers	Fetal Heart	heart
23	chr9:140483600-140484000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:140483600-140484000	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr9:140483600-140484000	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
26	chr9:140483600-140484000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr9:140483600-140484000	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr9:140483600-140484000	Enhancers	Primary B cells from peripheral blood	blood
29	chr9:140483600-140484000	Enhancers	Primary hematopoietic stem cells	blood
30	chr9:140483600-140484000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr9:140483600-140484000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
32	chr9:140483600-140484000	Enhancers	Fetal Brain Male	brain
33	chr9:140483600-140484000	Enhancers	Lung	lung
34	chr9:140483600-140484000	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr9:140483600-140484000	Enhancers	Spleen	Spleen
36	chr9:140483600-140484000	Flanking Active TSS	NHEK	skin
37	chr9:140483600-140484200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr9:140483600-140484200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr9:140483600-140484200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr9:140483600-140484200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr9:140483600-140484200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
42	chr9:140483600-140484200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr9:140483600-140484200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr9:140483600-140484200	Flanking Active TSS	HSMM	muscle
45	chr9:140483600-140484200	Flanking Active TSS	HUVEC	blood vessel
46	chr9:140483600-140484200	Flanking Active TSS	Osteobl	bone
47	chr9:140483600-140484400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr9:140483600-140484400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr9:140483600-140484400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
50	chr9:140483600-140484400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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