Variant report

Variant	nsv1041112
Chromosome Location	chr9:115960704-116005783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:894)
CpG islands
(count:307)
Chromatin interactive
region (count:65)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:894 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115990291-115990958	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:115993968-115994315	K562	blood:	n/a	n/a
3	ARID3A	chr9:115983506-115983747	K562	blood:	n/a	n/a
4	ARID3A	chr9:115983338-115984123	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:115984342-115985124	HepG2	liver:	n/a	n/a
6	ATF1	chr9:115990413-115990708	K562	blood:	n/a	n/a
7	ATF1	chr9:115983423-115983901	K562	blood:	n/a	n/a
8	ATF2	chr9:115983304-115984037	GM12878	blood:	n/a	chr9:115983730-115983741
9	ATF2	chr9:115983357-115983928	GM12878	blood:	n/a	chr9:115983730-115983741
10	ATF2	chr9:115981374-115982764	GM12878	blood:	n/a	n/a
11	ATF2	chr9:115983017-115983980	H1-hESC	embryonic stem cell:	n/a	chr9:115983730-115983741
12	ATF2	chr9:115981259-115982696	GM12878	blood:	n/a	n/a
13	ATF2	chr9:115983337-115983806	H1-hESC	embryonic stem cell:	n/a	chr9:115983730-115983741
14	ATF3	chr9:115983220-115983829	HepG2	liver:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
15	ATF3	chr9:115983301-115983851	H1-hESC	embryonic stem cell:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
16	ATF3	chr9:115983233-115983781	HepG2	liver:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
17	ATF3	chr9:115983419-115983792	H1-hESC	embryonic stem cell:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
18	ATF3	chr9:115983440-115983907	K562	blood:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
19	ATF3	chr9:115983213-115983792	GM12878	blood:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
20	ATF3	chr9:115983440-115983712	GM12878	blood:	n/a	n/a
21	ATF3	chr9:115984765-115985094	K562	blood:	n/a	n/a
22	ATF3	chr9:115983170-115983797	K562	blood:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
23	BACH1	chr9:115982879-115982887	K562	blood:	n/a	n/a
24	BACH1	chr9:115977469-115977786	K562	blood:	n/a	n/a
25	BACH1	chr9:115984091-115984099	K562	blood:	n/a	n/a
26	BACH1	chr9:115977514-115977791	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr9:115982206-115982623	GM12878	blood:	n/a	n/a
28	BATF	chr9:115982119-115982632	GM12878	blood:	n/a	n/a
29	BATF	chr9:115981439-115981805	GM12878	blood:	n/a	chr9:115981724-115981732
30	BATF	chr9:115981447-115981779	GM12878	blood:	n/a	chr9:115981724-115981732
31	BCL11A	chr9:115981417-115981873	GM12878	blood:	n/a	chr9:115981634-115981643
32	BCL11A	chr9:115982153-115982635	GM12878	blood:	n/a	n/a
33	BCLAF1	chr9:115981455-115982653	GM12878	blood:	n/a	chr9:115981634-115981643
34	BCLAF1	chr9:115983290-115983801	GM12878	blood:	n/a	chr9:115983759-115983768 chr9:115983750-115983763 chr9:115983606-115983615
35	BCLAF1	chr9:115981212-115982657	GM12878	blood:	n/a	chr9:115981634-115981643
36	BHLHE40	chr9:115990322-115990675	K562	blood:	n/a	n/a
37	BHLHE40	chr9:115983468-115983999	HepG2	liver:	n/a	n/a
38	BHLHE40	chr9:115990316-115990750	HepG2	liver:	n/a	n/a
39	BHLHE40	chr9:115983525-115983870	A549	lung:	n/a	n/a
40	BHLHE40	chr9:115984504-115984694	K562	blood:	n/a	n/a
41	BHLHE40	chr9:115981434-115981876	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:115995278-115995394	GM12878	blood:	n/a	n/a
43	BHLHE40	chr9:115982127-115984239	GM12878	blood:	n/a	chr9:115984103-115984119
44	BHLHE40	chr9:115982855-115984189	K562	blood:	n/a	chr9:115984103-115984119
45	BRCA1	chr9:115983701-115984066	HepG2	liver:	n/a	n/a
46	BRCA1	chr9:115984414-115984624	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr9:115983208-115984068	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr9:115983809-115983814	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr9:115983384-115983407	HepG2	liver:	n/a	n/a
50	CBX3	chr9:115983381-115984015	K562	blood:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115983984-115984034	Hela-S3	cervix:	n/a
2	chr9:115983984-115984034	NB4	blood:	n/a
3	chr9:115983984-115984034	Hela-S3	cervix:	n/a
4	chr9:115983984-115984034	NB4	blood:	n/a
5	chr9:115987035-115987085	HepG2	liver:	n/a
6	chr9:115984268-115984318	AG10803	skin:	n/a
7	chr9:115983636-115983686	A549	lung:	n/a
8	chr9:115983049-115983099	GM12891	blood:	n/a
9	chr9:115987035-115987085	PANC-1	pancreas:	n/a
10	chr9:115983984-115984034	LNCaP	prostate:	n/a
11	chr9:115987035-115987085	MCF-7	breast:	n/a
12	chr9:115983049-115983099	NHBE	bronchial:	n/a
13	chr9:115983636-115983686	GM12891	blood:	n/a
14	chr9:115983636-115983686	HRCEpiC	kidney:	n/a
15	chr9:115987035-115987085	CMK	blood:	n/a
16	chr9:115983636-115983686	PANC-1	pancreas:	n/a
17	chr9:115983049-115983099	HL-60	blood:	n/a
18	chr9:115987035-115987085	AG04449	skin:	fetal
19	chr9:115983049-115983099	A549	lung:	n/a
20	chr9:115983049-115983099	Hela-S3	cervix:	n/a
21	chr9:115987035-115987085	Hepatocyte	liver:	n/a
22	chr9:115984268-115984318	ovcar-3	ovarian:	n/a
23	chr9:115984268-115984318	SK-N-SH_RA	brain:	n/a
24	chr9:115983636-115983686	AG10803	skin:	n/a
25	chr9:115984268-115984318	IMR90	lung:	fetal
26	chr9:115987035-115987085	U87	brain:	n/a
27	chr9:115984268-115984318	NT2-D1	testis:	n/a
28	chr9:115983984-115984034	HRE	kidney:	n/a
29	chr9:115984268-115984318	GM12892	blood:	n/a
30	chr9:115983636-115983686	MCF10A-Er-Src	breast:	n/a
31	chr9:115987035-115987085	AG09319	gingival:	n/a
32	chr9:115984268-115984318	SAEC	small airway:	n/a
33	chr9:115983049-115983099	CMK	blood:	n/a
34	chr9:115984268-115984318	HRCEpiC	kidney:	n/a
35	chr9:115987035-115987085	NHDF-neo	bronchial:	n/a
36	chr9:115983636-115983686	GM12892	blood:	n/a
37	chr9:115984268-115984318	AoSMC	blood vessel:	n/a
38	chr9:115983984-115984034	A549	lung:	n/a
39	chr9:115983984-115984034	Caco-2	colon:	n/a
40	chr9:115983049-115983099	HCM	heart:	n/a
41	chr9:115983636-115983686	GM19239	blood:	n/a
42	chr9:115983636-115983686	PFSK-1	brain:	n/a
43	chr9:115983049-115983099	LNCaP	prostate:	n/a
44	chr9:115983636-115983686	ECC-1	luminal epithelium:	n/a
45	chr9:115983636-115983686	GM06990	blood:	n/a
46	chr9:115983984-115984034	AG04449	skin:	fetal
47	chr9:115983984-115984034	MCF-7	breast:	n/a
48	chr9:115984268-115984318	RPTEC	kidney:	n/a
49	chr9:115983984-115984034	BE2_C	brain:	n/a
50	chr9:115984268-115984318	Jurkat	blood:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:115988089..115990143-chr9:115997118..115999123,2	MCF-7	breast:
2	chr9:115995999..115998465-chr9:116001136..116003648,2	K562	blood:
3	chr9:115976079..115978566-chr9:116036874..116039120,2	MCF-7	breast:
4	chr9:115980360..115986264-chr9:116170629..116175189,6	K562	blood:
5	chr9:115959480..115961457-chr9:115966488..115968182,2	K562	blood:
6	chr9:115988910..115990516-chr9:115992954..115994537,2	MCF-7	breast:
7	chr9:115979271..115982033-chr9:115982056..115983606,2	MCF-7	breast:
8	chr9:116003514..116005216-chr9:116035646..116037704,2	MCF-7	breast:
9	chr9:115913327..115916086-chr9:115970304..115972231,2	MCF-7	breast:
10	chr9:115995531..115997450-chr9:115998162..116001080,2	MCF-7	breast:
11	chr9:115965291..115966796-chr9:115969248..115971645,2	K562	blood:
12	chr9:115978706..115980364-chr9:115981064..115982891,2	K562	blood:
13	chr9:115999423..116002068-chr9:116006233..116008819,2	K562	blood:
14	chr9:115993143..115995233-chr9:116002735..116005457,2	K562	blood:
15	chr9:115996965..115999527-chr9:116002148..116004164,2	K562	blood:
16	chr9:115974346..115976683-chr9:115980205..115982463,2	MCF-7	breast:
17	chr9:115995999..115998465-chr9:116001136..116003648,2	K562	blood:
18	chr9:115974346..115976683-chr9:115980205..115982463,2	MCF-7	breast:
19	chr9:115986078..115988319-chr9:115992917..115996032,3	MCF-7	breast:
20	chr9:115980759..115986590-chr9:115988652..115992433,8	K562	blood:
21	chr9:115991545..115993932-chr9:115995693..115997298,2	K562	blood:
22	chr9:115991545..115993932-chr9:115995693..115997298,2	K562	blood:
23	chr9:115961079..115963509-chr9:115965175..115968224,3	MCF-7	breast:
24	chr12:53894115..53894858-chr9:115983781..115984688,2	Hela-S3	cervix:
25	chr9:115995531..115997450-chr9:115998162..116001080,2	MCF-7	breast:
26	chr9:115978706..115980364-chr9:115981064..115982891,2	K562	blood:
27	chr9:115979802..115981343-chr9:115983049..115985677,2	K562	blood:
28	chr9:115982005..115986983-chr9:116035777..116039702,5	K562	blood:
29	chr9:115981081..115983502-chr9:115983537..115987172,3	MCF-7	breast:
30	chr9:115981837..115986059-chr9:115990865..115995580,5	MCF-7	breast:
31	chr9:115981728..115986983-chr9:116035777..116040437,9	K562	blood:
32	chr9:115983506..115986924-chr9:115988828..115991669,3	K562	blood:
33	chr9:115951377..115953931-chr9:115974239..115975925,2	MCF-7	breast:
34	chr9:115968725..115971196-chr9:115981878..115984279,2	MCF-7	breast:
35	chr9:115955703..115958661-chr9:115961003..115965387,3	MCF-7	breast:
36	chr9:115983573..115985886-chr9:115986006..115988568,3	MCF-7	breast:
37	chr9:115963672..115965977-chr9:115972388..115974143,2	MCF-7	breast:
38	chr9:115961079..115963509-chr9:115965175..115968224,3	MCF-7	breast:
39	chr9:115986078..115988319-chr9:115992917..115996032,3	MCF-7	breast:
40	chr9:115981852..115985156-chr9:116171660..116173942,3	MCF-7	breast:
41	chr9:115964326..115966174-chr9:115967230..115970062,3	MCF-7	breast:
42	chr9:115983607..115986374-chr9:116170251..116172763,3	MCF-7	breast:
43	chr9:115993143..115995233-chr9:116002735..116005457,2	K562	blood:
44	chr9:115952251..115954367-chr9:115960312..115963132,2	K562	blood:
45	chr9:115968725..115971196-chr9:115981878..115984279,2	MCF-7	breast:
46	chr9:116001272..116004183-chr9:116010675..116013051,2	MCF-7	breast:
47	chr9:115977770..115980066-chr9:115981974..115983622,2	MCF-7	breast:
48	chr9:115956014..115959253-chr9:115961029..115963531,3	K562	blood:
49	chr9:115988089..115990143-chr9:115997118..115999123,2	MCF-7	breast:
50	chr9:115990891..115993253-chr9:115993931..115999009,4	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDC26-2	chr9:115968291-115968858	NONHSAT134327
2	lnc-SLC31A1-1	chr9:115983808-115983958	NONHSAT134328
3	lnc-SLC31A1-1	chr9:115989558-115989940	NONHSAT134329
4	lnc-SLC31A1-1	chr9:115983867-115983958	NONHSAT134329
5	lnc-CDC26-2	chr9:115969492-115969576	NONHSAT134327

No data

Variant related genes	Relation type
FKBP15	TF binding region
SLC31A1	TF binding region
FKBP15	CpG island
SLC31A1	CpG island
ENSG00000148229	chromatin interactions
ENSG00000157653	chromatin interactions
ENSG00000136875	chromatin interactions
ENSG00000139546	chromatin interactions
ENSG00000167797	chromatin interactions
ENSG00000136868	chromatin interactions
ENSG00000119321	chromatin interactions
ENSG00000270175	chromatin interactions
ENSG00000176386	chromatin interactions

Extended variants
information (count: 1665 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1665 , 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	rs540019402	chr9:115960775-115960776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187884576	chr9:115960803-115960804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566410170	chr9:115960804-115960805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149134869	chr9:115960886-115960887	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535876252	chr9:115960900-115960901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550035954	chr9:115960920-115960921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7860472	chr9:115960956-115960957	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs572392054	chr9:115960986-115960987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148324933	chr9:115961027-115961028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7874583	chr9:115961059-115961060	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs374054178	chr9:115961095-115961096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371408857	chr9:115961124-115961125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374737007	chr9:115961126-115961127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141288448	chr9:115961131-115961132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372832505	chr9:115961143-115961144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375722025	chr9:115961153-115961154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369857780	chr9:115961166-115961167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374097177	chr9:115961170-115961171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377588392	chr9:115961183-115961184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369177721	chr9:115961197-115961198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550666306	chr9:115961203-115961204	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190235494	chr9:115961217-115961218	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376169190	chr9:115961245-115961246	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548402210	chr9:115961259-115961260	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562444006	chr9:115961283-115961284	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531473165	chr9:115961284-115961285	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146231385	chr9:115961306-115961307	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561380107	chr9:115961316-115961317	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182165229	chr9:115961319-115961320	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547219804	chr9:115961382-115961383	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570515737	chr9:115961387-115961388	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4407968	chr9:115961394-115961395	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs186815358	chr9:115961397-115961398	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374002328	chr9:115961427-115961428	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192305467	chr9:115961446-115961447	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536191270	chr9:115961544-115961545	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556073855	chr9:115961559-115961560	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4378033	chr9:115961618-115961619	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs535009689	chr9:115961691-115961692	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557980524	chr9:115961733-115961734	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552170556	chr9:115961737-115961738	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs55954029	chr9:115961751-115961752	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs533105776	chr9:115961755-115961756	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534659336	chr9:115961826-115961827	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4596714	chr9:115961853-115961854	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs185589877	chr9:115961856-115961857	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs111901736	chr9:115961928-115961929	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541746884	chr9:115961951-115961952	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368744416	chr9:115961974-115961975	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372183816	chr9:115962045-115962046	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1661 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115920000-115970200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:115920000-115973400	Strong transcription	Rectal Mucosa Donor 29	rectum
3	chr9:115920400-115973400	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr9:115920800-115966400	Strong transcription	Dnd41	blood
5	chr9:115920800-115975000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr9:115923400-115976400	Strong transcription	Primary T cells fromperipheralblood	blood
7	chr9:115924000-115965800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr9:115924200-115969600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr9:115927600-115973400	Strong transcription	Skeletal Muscle Female	skeletal muscle
10	chr9:115936800-115982400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr9:115941200-115968600	Strong transcription	Primary B cells from peripheral blood	blood
12	chr9:115941200-115969200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr9:115945400-115977200	Weak transcription	Stomach Mucosa	stomach
14	chr9:115945600-115982800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr9:115946000-115963600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr9:115949800-115961800	Weak transcription	Small Intestine	intestine
17	chr9:115950400-115972800	Weak transcription	Right Ventricle	heart
18	chr9:115950600-115968600	Weak transcription	Fetal Heart	heart
19	chr9:115950600-115982400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr9:115950800-115961800	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr9:115950800-115963400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr9:115950800-115963600	Weak transcription	Spleen	Spleen
23	chr9:115950800-115982800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:115951000-115972200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr9:115951000-115972200	Weak transcription	Gastric	stomach
26	chr9:115951000-115972200	Weak transcription	Pancreas	Pancrea
27	chr9:115951000-115974000	Strong transcription	Placenta	Placenta
28	chr9:115951000-115982800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr9:115951200-115964800	Weak transcription	Fetal Brain Male	brain
30	chr9:115951400-115961800	Weak transcription	NHEK	skin
31	chr9:115951400-115967800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr9:115952200-115968000	Strong transcription	GM12878-XiMat	blood
33	chr9:115952200-115974400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr9:115952400-115962600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr9:115952400-115962600	Strong transcription	Fetal Thymus	thymus
36	chr9:115952400-115962600	Strong transcription	Left Ventricle	heart
37	chr9:115952400-115965800	Strong transcription	Primary T cells from cord blood	blood
38	chr9:115952400-115973400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr9:115952400-115973600	Strong transcription	Adipose Nuclei	Adipose
40	chr9:115952400-115974400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr9:115953000-115961200	Weak transcription	Hela-S3	cervix
42	chr9:115953400-115967200	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr9:115953600-115967600	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr9:115954000-115965400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr9:115954600-115965200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr9:115954600-115973600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr9:115955600-115961400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr9:115956000-115973400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr9:115956200-115971800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr9:115956400-115962600	Strong transcription	HUES6 Cell Line	embryonic stem cell

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