Variant report

Variant	nsv613218
Chromosome Location	chr9:6697128-6724015
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:703)
CpG islands
(count:673)
Chromatin interactive
region (count:31)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6702813-6703015	K562	blood:	n/a	n/a
2	ARID3A	chr9:6714320-6714869	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6716174-6716454	HepG2	liver:	n/a	n/a
4	ATF2	chr9:6703987-6704605	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:6715844-6716527	GM12878	blood:	n/a	chr9:6716129-6716140
6	ATF2	chr9:6722741-6723673	GM12878	blood:	n/a	n/a
7	ATF2	chr9:6703874-6704656	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr9:6715890-6716329	GM12878	blood:	n/a	chr9:6716129-6716140
9	ATF2	chr9:6722727-6723186	GM12878	blood:	n/a	n/a
10	ATF2	chr9:6703839-6704309	GM12878	blood:	n/a	n/a
11	ATF2	chr9:6703375-6704596	GM12878	blood:	n/a	n/a
12	ATF3	chr9:6703972-6704567	H1-hESC	embryonic stem cell:	n/a	chr9:6704101-6704111
13	ATF3	chr9:6704051-6704512	A549	lung:	n/a	chr9:6704101-6704111
14	ATF3	chr9:6704072-6704352	GM12878	blood:	n/a	chr9:6704101-6704111
15	ATF3	chr9:6703937-6704598	GM12878	blood:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
16	ATF3	chr9:6703946-6704478	A549	lung:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
17	ATF3	chr9:6704052-6704432	HepG2	liver:	n/a	chr9:6704101-6704111
18	ATF3	chr9:6703900-6704493	H1-hESC	embryonic stem cell:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
19	ATF3	chr9:6703940-6704551	HepG2	liver:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
20	BACH1	chr9:6703514-6704556	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr9:6722711-6723091	GM12878	blood:	n/a	n/a
22	BATF	chr9:6723227-6723565	GM12878	blood:	n/a	n/a
23	BCL11A	chr9:6722699-6723018	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:6723143-6723561	GM12878	blood:	n/a	n/a
25	BCL3	chr9:6703922-6704535	A549	lung:	n/a	n/a
26	BCL3	chr9:6703998-6704656	A549	lung:	n/a	n/a
27	BCLAF1	chr9:6703280-6704665	GM12878	blood:	n/a	n/a
28	BCLAF1	chr9:6723281-6723701	GM12878	blood:	n/a	n/a
29	BCLAF1	chr9:6715879-6716683	GM12878	blood:	n/a	chr9:6716073-6716086 chr9:6716320-6716329 chr9:6716213-6716221
30	BCLAF1	chr9:6703931-6704678	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:6704046-6704437	A549	lung:	n/a	n/a
32	BHLHE40	chr9:6703524-6704514	GM12878	blood:	n/a	n/a
33	BHLHE40	chr9:6723433-6723669	GM12878	blood:	n/a	n/a
34	BHLHE40	chr9:6715802-6716907	HepG2	liver:	n/a	chr9:6716419-6716428 chr9:6716413-6716434 chr9:6716417-6716430 chr9:6716418-6716427 chr9:6716419-6716428
35	BHLHE40	chr9:6704026-6704494	HepG2	liver:	n/a	n/a
36	BHLHE40	chr9:6704234-6704320	K562	blood:	n/a	n/a
37	BHLHE40	chr9:6715913-6716873	GM12878	blood:	n/a	chr9:6716419-6716428 chr9:6716413-6716434 chr9:6716417-6716430 chr9:6716418-6716427 chr9:6716419-6716428
38	BRCA1	chr9:6715949-6716503	GM12878	blood:	n/a	n/a
39	BRCA1	chr9:6702904-6703133	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr9:6716101-6716288	HepG2	liver:	n/a	n/a
41	BRCA1	chr9:6704412-6704466	GM12878	blood:	n/a	n/a
42	CBX3	chr9:6708746-6709217	HCT-116	colon:	n/a	n/a
43	CEBPB	chr9:6715903-6716177	K562	blood:	n/a	chr9:6715961-6715972
44	CEBPB	chr9:6715203-6715509	K562	blood:	n/a	chr9:6715355-6715366
45	CEBPB	chr9:6715155-6715503	MCF-7	breast:	n/a	chr9:6715355-6715366
46	CEBPB	chr9:6705780-6705986	HepG2	liver:	n/a	chr9:6705845-6705856 chr9:6705846-6705857 chr9:6705809-6705821 chr9:6705845-6705858
47	CEBPB	chr9:6711405-6711761	IMR90	lung:	n/a	n/a
48	CEBPB	chr9:6713984-6714106	IMR90	lung:	n/a	n/a
49	CEBPB	chr9:6715856-6716204	HepG2	liver:	n/a	chr9:6715961-6715972
50	CEBPB	chr9:6714351-6714473	K562	blood:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6704574-6704624	HAEpiC	amniotic membrane:	n/a
2	chr9:6706149-6706199	NHDF-neo	bronchial:	n/a
3	chr9:6704574-6704624	HAEpiC	amniotic membrane:	n/a
4	chr9:6706149-6706199	NHDF-neo	bronchial:	n/a
5	chr9:6716007-6716057	AG04449	skin:	fetal
6	chr9:6703605-6703655	ProgFib	skin:	n/a
7	chr9:6716480-6716530	HCPEpiC	choroid plexus:	n/a
8	chr9:6716480-6716530	MCF-7	breast:	n/a
9	chr9:6706149-6706199	IMR90	lung:	fetal
10	chr9:6703949-6703999	GM12891	blood:	n/a
11	chr9:6716417-6716467	AG10803	skin:	n/a
12	chr9:6703949-6703999	HCT-116	colon:	n/a
13	chr9:6707115-6707165	HCF	heart:	n/a
14	chr9:6704178-6704228	PrEC	prostate:	n/a
15	chr9:6704178-6704228	NH-A	brain:	n/a
16	chr9:6703605-6703655	HNPCEpiC	eye:	n/a
17	chr9:6703605-6703655	AG09319	gingival:	n/a
18	chr9:6704574-6704624	HPAEpiC	pulmonary alveolar:	n/a
19	chr9:6716480-6716530	GM12891	blood:	n/a
20	chr9:6716007-6716057	HUVEC	blood vessel:	n/a
21	chr9:6703605-6703655	HEK293	kidney:	embryo
22	chr9:6707115-6707165	PrEC	prostate:	n/a
23	chr9:6715032-6715082	IMR90	lung:	fetal
24	chr9:6704178-6704228	HRE	kidney:	n/a
25	chr9:6704574-6704624	GM12878	blood:	n/a
26	chr9:6703949-6703999	K562	blood:	n/a
27	chr9:6703605-6703655	HCT-116	colon:	n/a
28	chr9:6704574-6704624	U87	brain:	n/a
29	chr9:6716417-6716467	AG09319	gingival:	n/a
30	chr9:6700000-6700050	AG09319	gingival:	n/a
31	chr9:6707115-6707165	MCF-7	breast:	n/a
32	chr9:6715032-6715082	GM19239	blood:	n/a
33	chr9:6706149-6706199	K562	blood:	n/a
34	chr9:6703605-6703655	GM19239	blood:	n/a
35	chr9:6715032-6715082	LNCaP	prostate:	n/a
36	chr9:6704574-6704624	GM06990	blood:	n/a
37	chr9:6716007-6716057	HRE	kidney:	n/a
38	chr9:6716007-6716057	LNCaP	prostate:	n/a
39	chr9:6715032-6715082	HUVEC	blood vessel:	n/a
40	chr9:6716480-6716530	ECC-1	luminal epithelium:	n/a
41	chr9:6700000-6700050	GM12892	blood:	n/a
42	chr9:6716007-6716057	PFSK-1	brain:	n/a
43	chr9:6716480-6716530	HEK293	kidney:	embryo
44	chr9:6704178-6704228	ProgFib	skin:	n/a
45	chr9:6703949-6703999	ProgFib	skin:	n/a
46	chr9:6704178-6704228	AoSMC	blood vessel:	n/a
47	chr9:6703949-6703999	SKMC	muscle:	n/a
48	chr9:6707115-6707165	NHDF-neo	bronchial:	n/a
49	chr9:6703949-6703999	RPTEC	kidney:	n/a
50	chr9:6704574-6704624	T-47D	breast:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6722888..6726785-chr9:6754807..6757177,3	K562	blood:
2	chr9:6713012..6714984-chr9:6718479..6720574,2	K562	blood:
3	chr9:6690536..6693350-chr9:6698647..6700189,2	MCF-7	breast:
4	chr14:51410899..51411829-chr9:6715512..6716484,2	HCT-116	colon:
5	chr21:41708247..41710641-chr9:6714300..6715810,2	MCF-7	breast:
6	chr9:6702847..6705575-chr9:6714326..6717882,7	MCF-7	breast:
7	chr9:6698340..6700152-chr9:6701946..6704339,2	MCF-7	breast:
8	chr9:6702847..6705575-chr9:6714326..6717882,7	MCF-7	breast:
9	chr9:6698340..6700152-chr9:6701946..6704339,2	MCF-7	breast:
10	chr9:6714309..6715981-chr9:6723655..6726584,2	MCF-7	breast:
11	chr1:100503108..100504085-chr9:6716038..6716673,2	NB4	blood:
12	chr5:166255725..166256712-chr9:6703618..6704233,2	MCF-7	breast:
13	chr9:6683289..6684884-chr9:6702645..6704262,2	MCF-7	breast:
14	chr9:6715258..6717463-chr9:6718537..6720528,2	MCF-7	breast:
15	chr9:6714844..6717578-chr9:6754943..6759087,4	MCF-7	breast:
16	chr9:6714309..6715981-chr9:6723655..6726584,2	MCF-7	breast:
17	chr2:32389334..32390859-chr9:6713099..6716031,2	MCF-7	breast:
18	chr9:6706468..6709007-chr9:6764056..6766511,2	MCF-7	breast:
19	chr9:6690617..6692723-chr9:6701607..6704265,2	MCF-7	breast:
20	chr9:6702391..6705446-chr9:6756717..6760058,5	MCF-7	breast:
21	chr9:6702551..6705246-chr9:6715022..6717677,6	MCF-7	breast:
22	chr9:6715258..6717463-chr9:6718537..6720528,2	MCF-7	breast:
23	chr9:6711589..6718151-chr9:6755774..6759657,12	MCF-7	breast:
24	chr5:166256227..166256733-chr9:6703705..6704305,2	MCF-7	breast:
25	chr9:6685820..6688107-chr9:6699923..6703311,3	MCF-7	breast:
26	chr9:6681423..6683704-chr9:6710640..6713020,2	MCF-7	breast:
27	chr9:6682207..6684667-chr9:6707689..6709841,2	K562	blood:
28	chr9:6681451..6683371-chr9:6705864..6707945,2	MCF-7	breast:
29	chr9:6699861..6702298-chr9:6702749..6705225,2	MCF-7	breast:
30	chr9:6702551..6705246-chr9:6715022..6717677,6	MCF-7	breast:
31	chr9:6686168..6688293-chr9:6706461..6708275,2	MCF-7	breast:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-2	chr9:6704471-6704653	XLOC_007275
2	lnc-KDM4C-1	chr9:6716183-6716616	NONHSAT130157
3	lnc-KDM4C-1	chr9:6708810-6708981	NONHSAT130155
4	lnc-KDM4C-1	chr9:6719071-6719154	ENSG00000225489.2
5	lnc-KDM4C-1	chr9:6717873-6718149	NONHSAT130158
6	lnc-KDM4C-1	chr9:6723527-6723630	ENSG00000225489.1
7	lnc-KDM4C-1	chr9:6710863-6710997	NONHSAT130156
8	lnc-KDM4C-1	chr9:6710863-6710997	NONHSAT130154
9	lnc-KDM4C-1	chr9:6709071-6709370	NONHSAT130155
10	lnc-KDM4C-2	chr9:6707542-6707776	NONHSAT130153
11	lnc-KDM4C-2	chr9:6704453-6704977	NONHSAT130152
12	lnc-KDM4C-1	chr9:6716196-6716315	NONHSAT130158
13	lnc-KDM4C-1	chr9:6709068-6709154	NONHSAT130156
14	lnc-KDM4C-1	chr9:6719068-6719154	ENSG00000225489.1
15	lnc-KDM4C-2	chr9:6704339-6704366	NONHSAT130152
16	lnc-KDM4C-11	chr9:6697542-6697780	NONHSAT130150
17	lnc-KDM4C-1	chr9:6716946-6717438	NONHSAT130156
18	lnc-KDM4C-1	chr9:6716503-6716619	NONHSAT130156
19	lnc-KDM4C-1	chr9:6709071-6709154	NONHSAT130154
20	lnc-KDM4C-1	chr9:6717873-6719234	NONHSAT130157
21	lnc-KDM4C-2	chr9:6707542-6707763	XLOC_007275
22	lnc-KDM4C-2	chr9:6704453-6704653	XLOC_007275
23	lnc-KDM4C-1	chr9:6720863-6720997	ENSG00000225489.1
24	lnc-KDM4C-1	chr9:6717873-6718981	ENSG00000225489.1
25	lnc-KDM4C-2	chr9:6704406-6704653	NONHSAT130153
26	lnc-KDM4C-1	chr9:6720863-6720997	ENSG00000225489.1
27	lnc-KDM4C-1	chr9:6718810-6718981	ENSG00000225489.1
28	lnc-KDM4C-1	chr9:6716548-6716616	ENSG00000225489.1
29	lnc-KDM4C-1	chr9:6720863-6720997	ENSG00000225489.2
30	lnc-KDM4C-1	chr9:6706548-6706616	NONHSAT130154
31	lnc-KDM4C-1	chr9:6718965-6718981	ENSG00000225489.2
32	lnc-KDM4C-1	chr9:6707873-6708981	NONHSAT130154
33	lnc-KDM4C-1	chr9:6719071-6719370	ENSG00000225489.1
34	lnc-KDM4C-2	chr9:6707542-6707780	XLOC_007275
35	lnc-KDM4C-2	chr9:6704179-6704343	XLOC_007275
36	lnc-KDM4C-1	chr9:6719071-6719154	ENSG00000225489.1
37	lnc-KDM4C-1	chr9:6713527-6713630	NONHSAT130154

No data

Variant related genes	Relation type
ENSG00000225489	TF binding region
ENSG00000229611	TF binding region
KDM4C	TF binding region
ENSG00000225489	CpG island
ENSG00000229611	CpG island
KDM4C	CpG island
ENSG00000107077	chromatin interactions
ENSG00000156875	chromatin interactions
ENSG00000100504	chromatin interactions
ENSG00000225489	chromatin interactions
ENSG00000272716	chromatin interactions
ENSG00000229611	chromatin interactions
DNMT3A	miRNA target sites
NXT2	miRNA target sites

Extended variants
information (count: 1454 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1454 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10739110	chr9:6697128-6697129	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575867998	chr9:6697163-6697164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544010301	chr9:6697204-6697205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562112460	chr9:6697226-6697227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529600813	chr9:6697249-6697250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547727121	chr9:6697348-6697349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368677772	chr9:6697353-6697354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533147677	chr9:6697361-6697362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551496235	chr9:6697411-6697412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569795761	chr9:6697412-6697413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544496559	chr9:6697423-6697424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374560195	chr9:6697468-6697469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190955997	chr9:6697479-6697480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535741631	chr9:6697494-6697495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372953607	chr9:6697497-6697498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377210963	chr9:6697556-6697557	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs553777299	chr9:6697559-6697560	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs572046311	chr9:6697562-6697563	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs111658796	chr9:6697563-6697564	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs557914517	chr9:6697604-6697605	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs576226856	chr9:6697635-6697636	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs543503138	chr9:6697657-6697658	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs555181270	chr9:6697664-6697665	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs574915030	chr9:6697673-6697674	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs368099111	chr9:6697718-6697719	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs535664906	chr9:6697740-6697741	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs71330119	chr9:6697741-6697742	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs112446282	chr9:6697742-6697743	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs562311465	chr9:6697750-6697751	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs369678383	chr9:6697829-6697830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs820514	chr9:6697836-6697837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs182291070	chr9:6697854-6697855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560170285	chr9:6697886-6697887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559782246	chr9:6697916-6697917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533184245	chr9:6697934-6697935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551385482	chr9:6697937-6697938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140151924	chr9:6697947-6697948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532372929	chr9:6697967-6697968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530919097	chr9:6697989-6697990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs202231590	chr9:6697997-6697998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549159269	chr9:6698023-6698024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187351869	chr9:6698051-6698052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192356051	chr9:6698077-6698078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs820515	chr9:6698085-6698086	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs539715786	chr9:6698086-6698087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555583574	chr9:6698108-6698109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182783312	chr9:6698126-6698127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576060642	chr9:6698135-6698136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537197258	chr9:6698156-6698157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555162060	chr9:6698216-6698217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6682600-6703200	Weak transcription	Thymus	Thymus
2	chr9:6682600-6703600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:6683600-6703200	Weak transcription	Fetal Muscle Leg	muscle
4	chr9:6692000-6703400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr9:6693600-6702800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:6695800-6703000	Weak transcription	Primary B cells from cord blood	blood
7	chr9:6696800-6702800	Weak transcription	Primary B cells from peripheral blood	blood
8	chr9:6702200-6702800	Enhancers	GM12878-XiMat	blood
9	chr9:6702200-6703600	Enhancers	Hela-S3	cervix
10	chr9:6702400-6703000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr9:6702600-6702800	Weak transcription	A549	lung
12	chr9:6702800-6703000	Enhancers	A549	lung
13	chr9:6702800-6703200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:6702800-6703200	Enhancers	Primary B cells from peripheral blood	blood
15	chr9:6702800-6703400	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr9:6702800-6703600	Flanking Active TSS	GM12878-XiMat	blood
17	chr9:6703000-6703200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr9:6703000-6703200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr9:6703000-6703200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr9:6703000-6703200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr9:6703000-6703200	Enhancers	Primary T cells from cord blood	blood
22	chr9:6703000-6703200	Active TSS	Primary hematopoietic stem cells	blood
23	chr9:6703000-6703200	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr9:6703000-6703200	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr9:6703000-6703200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr9:6703000-6703200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr9:6703000-6703200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr9:6703000-6703200	Enhancers	Colonic Mucosa	Colon
29	chr9:6703000-6703200	Enhancers	Duodenum Mucosa	Duodenum
30	chr9:6703000-6703200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr9:6703000-6703200	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr9:6703000-6703200	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr9:6703000-6703200	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr9:6703000-6703400	Active TSS	H1 Cell Line	embryonic stem cell
35	chr9:6703000-6703400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr9:6703000-6703400	Flanking Active TSS	A549	lung
37	chr9:6703000-6703800	Flanking Active TSS	Primary B cells from cord blood	blood
38	chr9:6703000-6704600	Active TSS	Primary T killer memory cells from peripheral blood	blood
39	chr9:6703000-6704600	Active TSS	Placenta Amnion	Placenta Amnion
40	chr9:6703200-6703400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr9:6703200-6703400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
42	chr9:6703200-6703400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr9:6703200-6703400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr9:6703200-6703400	Enhancers	Primary T cells fromperipheralblood	blood
45	chr9:6703200-6703400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr9:6703200-6703400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr9:6703200-6703400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr9:6703200-6703400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr9:6703200-6703400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr9:6703200-6703400	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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