Variant report

Variant	nsv1044418
Chromosome Location	chr9:140686097-141005637
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2987)
CpG islands
(count:4340)
Chromatin interactive
region (count:131)
LncRNA
region (count:26)
Mature miRNA
region (count: 1)
miRNA target
sites (count:3)

(count:2987 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:140884817-140885010	K562	blood:	n/a	n/a
2	ATF2	chr9:140710777-140711402	GM12878	blood:	n/a	n/a
3	ATF2	chr9:140703449-140703804	GM12878	blood:	n/a	n/a
4	ATF2	chr9:140761215-140761514	GM12878	blood:	n/a	n/a
5	ATF2	chr9:140710782-140711539	GM12878	blood:	n/a	n/a
6	ATF3	chr9:140772100-140772314	K562	blood:	n/a	chr9:140772176-140772196
7	ATF3	chr9:140851195-140851422	K562	blood:	n/a	n/a
8	ATF3	chr9:140772113-140772351	H1-hESC	embryonic stem cell:	n/a	chr9:140772176-140772196
9	BACH1	chr9:140918133-140918313	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:140778170-140778249	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr9:140773050-140773062	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr9:140710900-140711326	GM12878	blood:	n/a	chr9:140711120-140711131
13	BATF	chr9:140747930-140748125	GM12878	blood:	n/a	n/a
14	BATF	chr9:140710702-140711592	GM12878	blood:	n/a	chr9:140711120-140711131
15	BATF	chr9:140761031-140761428	GM12878	blood:	n/a	n/a
16	BATF	chr9:140768794-140769134	GM12878	blood:	n/a	n/a
17	BATF	chr9:140731105-140731321	GM12878	blood:	n/a	n/a
18	BATF	chr9:140768772-140769151	GM12878	blood:	n/a	n/a
19	BCL11A	chr9:140720112-140720348	GM12878	blood:	n/a	chr9:140720260-140720269
20	BCL11A	chr9:140710826-140711435	GM12878	blood:	n/a	n/a
21	BCL11A	chr9:140768831-140769188	GM12878	blood:	n/a	n/a
22	BCL11A	chr9:140761035-140761355	GM12878	blood:	n/a	n/a
23	BCL11A	chr9:140768767-140769277	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:140703488-140703846	GM12878	blood:	n/a	n/a
25	BCL3	chr9:140760724-140761478	GM12878	blood:	n/a	n/a
26	BCL3	chr9:140904990-140905244	GM12878	blood:	n/a	n/a
27	BCL3	chr9:140707704-140708126	GM12878	blood:	n/a	n/a
28	BCL3	chr9:140910358-140910716	GM12878	blood:	n/a	n/a
29	BCL3	chr9:140707638-140708059	GM12878	blood:	n/a	n/a
30	BCL3	chr9:140702187-140702477	GM12878	blood:	n/a	n/a
31	BCL3	chr9:140993643-140993893	GM12878	blood:	n/a	n/a
32	BCL3	chr9:140699190-140700049	GM12878	blood:	n/a	n/a
33	BCL3	chr9:140910297-140910754	GM12878	blood:	n/a	n/a
34	BCL3	chr9:140699230-140700056	GM12878	blood:	n/a	n/a
35	BCLAF1	chr9:140710805-140711566	GM12878	blood:	n/a	n/a
36	BCLAF1	chr9:140703525-140703782	GM12878	blood:	n/a	n/a
37	BCLAF1	chr9:140703419-140703881	GM12878	blood:	n/a	n/a
38	BHLHE40	chr9:140782765-140782847	K562	blood:	n/a	n/a
39	BHLHE40	chr9:140851240-140851513	HepG2	liver:	n/a	n/a
40	BHLHE40	chr9:140948939-140949175	HepG2	liver:	n/a	n/a
41	BHLHE40	chr9:140948945-140949242	K562	blood:	n/a	n/a
42	BHLHE40	chr9:140851209-140851501	GM12878	blood:	n/a	n/a
43	BHLHE40	chr9:140993839-140994191	K562	blood:	n/a	n/a
44	BHLHE40	chr9:140760778-140760955	GM12878	blood:	n/a	n/a
45	BHLHE40	chr9:140879411-140879615	HepG2	liver:	n/a	n/a
46	BHLHE40	chr9:140772955-140773232	K562	blood:	n/a	chr9:140773100-140773109
47	BHLHE40	chr9:140731130-140731329	K562	blood:	n/a	n/a
48	BHLHE40	chr9:140862896-140863013	K562	blood:	n/a	n/a
49	BHLHE40	chr9:140710980-140711476	GM12878	blood:	n/a	n/a
50	BHLHE40	chr9:140851159-140851515	K562	blood:	n/a	n/a

(count:4340 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140728491-140728541	Jurkat	blood:	n/a
2	chr9:140957018-140957068	Hepatocyte	liver:	n/a
3	chr9:140727297-140727347	AG10803	skin:	n/a
4	chr9:140709033-140709083	RPTEC	kidney:	n/a
5	chr9:140815010-140815060	AG04449	skin:	fetal
6	chr9:140818325-140818375	HUVEC	blood vessel:	n/a
7	chr9:140815010-140815060	HEEpiC	esophagus:	n/a
8	chr9:140916078-140916128	GM06990	blood:	n/a
9	chr9:140780551-140780601	MCF-7	breast:	n/a
10	chr9:140728491-140728541	Jurkat	blood:	n/a
11	chr9:140957018-140957068	Hepatocyte	liver:	n/a
12	chr9:140727297-140727347	AG10803	skin:	n/a
13	chr9:140709033-140709083	RPTEC	kidney:	n/a
14	chr9:140815010-140815060	AG04449	skin:	fetal
15	chr9:140818325-140818375	HUVEC	blood vessel:	n/a
16	chr9:140815010-140815060	HEEpiC	esophagus:	n/a
17	chr9:140916078-140916128	GM06990	blood:	n/a
18	chr9:140780551-140780601	MCF-7	breast:	n/a
19	chr9:140731445-140731495	HEEpiC	esophagus:	n/a
20	chr9:140916078-140916128	NB4	blood:	n/a
21	chr9:140916980-140917030	CMK	blood:	n/a
22	chr9:140731445-140731495	GM06990	blood:	n/a
23	chr9:140729241-140729291	MCF-7	breast:	n/a
24	chr9:140735058-140735108	HMEC	breast:	n/a
25	chr9:140735058-140735108	GM19239	blood:	n/a
26	chr9:140771661-140771711	AG09309	skin:	n/a
27	chr9:140704065-140704115	NT2-D1	testis:	n/a
28	chr9:140707378-140707428	MCF10A-Er-Src	breast:	n/a
29	chr9:140727571-140727621	NH-A	brain:	n/a
30	chr9:140942584-140942634	Caco-2	colon:	n/a
31	chr9:140712932-140712982	AG09309	skin:	n/a
32	chr9:140733714-140733764	MCF10A-Er-Src	breast:	n/a
33	chr9:140703637-140703687	H1-hESC	embryonic stem cell:	embryo
34	chr9:140815937-140815987	BE2_C	brain:	n/a
35	chr9:140705990-140706040	AG10803	skin:	n/a
36	chr9:140687144-140687194	MCF-7	breast:	n/a
37	chr9:140728491-140728541	BJ	skin:	n/a
38	chr9:140711975-140712025	A549	lung:	n/a
39	chr9:140916980-140917030	NHDF-neo	bronchial:	n/a
40	chr9:140716770-140716820	Caco-2	colon:	n/a
41	chr9:140732731-140732781	Hela-S3	cervix:	n/a
42	chr9:140731445-140731495	H1-hESC	embryonic stem cell:	embryo
43	chr9:140726863-140726913	HCT-116	colon:	n/a
44	chr9:140735058-140735108	AG09309	skin:	n/a
45	chr9:140705990-140706040	GM12878	blood:	n/a
46	chr9:140703637-140703687	MCF-7	breast:	n/a
47	chr9:140771990-140772040	AG04449	skin:	fetal
48	chr9:140787445-140787495	PFSK-1	brain:	n/a
49	chr9:140773129-140773179	ProgFib	skin:	n/a
50	chr9:140970188-140970238	GM19239	blood:	n/a

(count:131 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:140875871..140879281-chr9:140879997..140882583,3	MCF-7	breast:
2	chr9:140713786..140716725-chr9:140719882..140722951,3	K562	blood:
3	chr9:140949053..140949565-chr9:140995304..140996092,3	MCF-7	breast:
4	chr9:140949053..140949565-chr9:140995304..140996092,3	MCF-7	breast:
5	chr22:50714431..50715299-chr9:140947514..140948493,3	MCF-7	breast:
6	chr9:140778196..140781664-chr9:140782755..140784568,3	K562	blood:
7	chr9:140700744..140703518-chr9:140712352..140715179,2	K562	blood:
8	chr9:140706148..140707731-chr9:140712808..140715644,2	K562	blood:
9	chr9:140725074..140728358-chr9:140730980..140733506,3	K562	blood:
10	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
11	chr9:140692420..140694081-chr9:140698871..140701591,2	K562	blood:
12	chr9:140960893..140963806-chr9:140965235..140966903,2	K562	blood:
13	chr9:140860566..140865150-chr9:140867846..140870803,4	MCF-7	breast:
14	chr9:140862016..140865668-chr9:140879753..140883106,4	MCF-7	breast:
15	chr9:140797540..140799636-chr9:140804864..140807689,2	K562	blood:
16	chr9:140718370..140720341-chr9:140724405..140727123,2	MCF-7	breast:
17	chr9:140700744..140703518-chr9:140712352..140715179,2	K562	blood:
18	chr9:140909435..140911470-chr9:140917464..140919841,2	MCF-7	breast:
19	chr9:140700980..140705198-chr9:140707876..140710677,3	K562	blood:
20	chr9:140991128..140993433-chr9:140998381..141000455,2	K562	blood:
21	chr14:100197709..100198229-chr9:140777193..140778054,2	MCF-7	breast:
22	chr9:140900853..140903158-chr9:140909684..140912170,2	MCF-7	breast:
23	chr9:140844057..140846982-chr9:140852715..140855154,2	MCF-7	breast:
24	chr9:140770577..140775397-chr9:140776407..140782162,11	K562	blood:
25	chr9:140914118..140916387-chr9:140964722..140966318,2	MCF-7	breast:
26	chr9:140705835..140707524-chr9:140709188..140711003,2	K562	blood:
27	chr9:140870732..140873052-chr9:140876120..140877929,2	K562	blood:
28	chr9:140796431..140799040-chr9:140804864..140806682,2	K562	blood:
29	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
30	chr9:140914118..140916387-chr9:140964722..140966318,2	MCF-7	breast:
31	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
32	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
33	chr9:140844057..140846982-chr9:140852715..140855154,2	MCF-7	breast:
34	chr9:140860566..140865150-chr9:140867846..140870803,4	MCF-7	breast:
35	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
36	chr9:140930141..140932633-chr9:140940366..140943124,2	MCF-7	breast:
37	chr9:140732797..140735433-chr9:140735710..140738705,2	MCF-7	breast:
38	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
39	chr9:140720128..140722152-chr9:140723312..140725717,2	K562	blood:
40	chr9:140955879..140956683-chr9:140995540..140996190,2	MCF-7	breast:
41	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
42	chr9:140952348..140955305-chr9:140964883..140967739,2	MCF-7	breast:
43	chr9:140966280..140969244-chr9:140971233..140973098,3	K562	blood:
44	chr9:140966280..140969244-chr9:140971430..140973098,2	K562	blood:
45	chr9:140869140..140872298-chr9:140874733..140877130,3	MCF-7	breast:
46	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
47	chr9:140960893..140963806-chr9:140965235..140966903,2	K562	blood:
48	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
49	chr9:140865657..140867593-chr9:140877024..140879679,2	MCF-7	breast:
50	chr9:140963638..140966246-chr9:140975970..140978505,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL772363.1-1	chr9:140762365-140762689	XLOC_007904
2	lnc-AL772363.1-1	chr9:140767517-140767710	XLOC_007904
3	lnc-AL772363.1-1	chr9:140784498-140787022	ENSG00000203987.2
4	lnc-AL772363.1-7	chr9:140954809-140955130	NONHSAT135765
5	lnc-AL772363.1-7	chr9:140955477-140955599	NONHSAT135765
6	lnc-AL772363.1-6	chr9:140939331-140939523	NONHSAT135763
7	lnc-AL772363.1-1	chr9:140767616-140767710	XLOC_007904
8	lnc-AL772363.1-1	chr9:140769915-140770844	XLOC_007904
9	lnc-AL772363.1-1	chr9:140762377-140762689	ENSG00000203987.2
10	lnc-AL772363.1-1	chr9:140771009-140771749	XLOC_007904
11	lnc-AL772363.1-1	chr9:140769915-140770132	XLOC_007904
12	lnc-AL772363.1-1	chr9:140768516-140768684	XLOC_007904
13	lnc-AL772363.1-1	chr9:140768516-140768684	XLOC_007904
14	lnc-AL772363.1-7	chr9:140954806-140956852	NONHSAT135764
15	lnc-AL772363.1-1	chr9:140768516-140768666	ENSG00000203987.2
16	lnc-AL772363.1-1	chr9:140762379-140762689	ENSG00000203987.2
17	lnc-AL772363.1-6	chr9:140937901-140938239	NONHSAT135763
18	lnc-AL772363.1-6	chr9:140934955-140937453	NONHSAT135763
19	lnc-AL772363.1-1	chr9:140771009-140771749	XLOC_007904
20	lnc-AL772363.1-4	chr9:140703295-140703875	NONHSAT135753
21	lnc-AL772363.1-1	chr9:140769915-140770132	ENSG00000203987.2
22	lnc-AL772363.1-1	chr9:140769915-140770132	XLOC_007904
23	lnc-AL772363.1-3	chr9:140843115-140843211	NONHSAT135761
24	lnc-AL772363.1-1	chr9:140768516-140768684	XLOC_007904
25	lnc-AL772363.1-3	chr9:140843618-140844002	NONHSAT135761
26	lnc-AL772363.1-1	chr9:140777289-140777454	ENSG00000203987.2

miRNA name	Chromosome Location	mirBase accession
hsa-miR-602	chr9:140732886-140732908	MIMAT0003270

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	EHMT1	hsa-miR-1	chr9:140730432-140730455
2	EHMT1	hsa-miR-30e-5p	chr9:140730456-140730473
3	EHMT1	hsa-miR-615-3p	chr9:140729903-140729924

Variant related genes	Relation type
ENSG00000203987	TF binding region
MIR602	TF binding region
EHMT1	TF binding region
ENSG00000255585	TF binding region
CACNA1B	TF binding region
ENSG00000203987	CpG island
MIR602	CpG island
EHMT1	CpG island
ENSG00000255585	CpG island
CACNA1B	CpG island
ENSG00000181090	chromatin interactions
ENSG00000207693	chromatin interactions
ENSG00000148399	chromatin interactions
ENSG00000148408	chromatin interactions
ENSG00000206737	chromatin interactions
PRRG1	miRNA target sites
AKAP11	miRNA target sites
GPM6A	miRNA target sites
ACIN1	miRNA target sites

Extended variants
information (count: 14049 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:14049 , 50 per page) page: 1 2 3 4 5 6 7 ... 281

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140687217	chr9:140686196-140686197	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577494657	chr9:140686227-140686228	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111284267	chr9:140686243-140686244	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556780893	chr9:140686253-140686254	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576584774	chr9:140686264-140686265	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531212254	chr9:140686269-140686270	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10867071	chr9:140686293-140686294	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs567658200	chr9:140686296-140686297	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113382187	chr9:140686304-140686305	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192183022	chr9:140686330-140686331	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs111565382	chr9:140686356-140686357	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs10867072	chr9:140686373-140686374	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs532473422	chr9:140686385-140686386	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552205913	chr9:140686396-140686397	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185713743	chr9:140686404-140686405	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531410242	chr9:140686450-140686451	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139777722	chr9:140686484-140686485	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568258221	chr9:140686560-140686561	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79635856	chr9:140686568-140686569	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547421822	chr9:140686580-140686581	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553449947	chr9:140686659-140686660	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187711313	chr9:140686725-140686726	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192517543	chr9:140686752-140686753	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184698140	chr9:140686769-140686770	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556584052	chr9:140686801-140686802	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570289488	chr9:140686862-140686863	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75485587	chr9:140686867-140686868	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555993993	chr9:140686881-140686882	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566827120	chr9:140686882-140686883	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574615901	chr9:140686895-140686896	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540317592	chr9:140686912-140686913	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553798631	chr9:140687006-140687007	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576786277	chr9:140687033-140687034	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545740965	chr9:140687048-140687049	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538857524	chr9:140687081-140687082	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111370430	chr9:140687101-140687102	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139583558	chr9:140687108-140687109	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112791882	chr9:140687113-140687114	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4876943	chr9:140687122-140687123	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs527449313	chr9:140687161-140687162	Strong transcription Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs149714961	chr9:140687172-140687173	Strong transcription Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs58646482	chr9:140687212-140687213	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548056921	chr9:140687220-140687221	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369391655	chr9:140687221-140687222	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570878995	chr9:140687253-140687254	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372273877	chr9:140687266-140687267	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146707506	chr9:140687296-140687297	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570300440	chr9:140687315-140687316	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544099818	chr9:140687402-140687403	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374522237	chr9:140687410-140687411	Strong transcription Weak transcription Genic enhancers	n/a	n/a	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:3227 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140649800-140712400	Weak transcription	Psoas Muscle	Psoas
2	chr9:140650200-140700000	Strong transcription	Primary T cells from cord blood	blood
3	chr9:140664200-140698600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr9:140664200-140701000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr9:140664600-140708000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr9:140664800-140700000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr9:140665000-140700000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr9:140665200-140702000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr9:140665400-140697800	Strong transcription	Thymus	Thymus
10	chr9:140665400-140700800	Strong transcription	Fetal Stomach	stomach
11	chr9:140667200-140698000	Strong transcription	Dnd41	blood
12	chr9:140667200-140699000	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr9:140668200-140698000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr9:140668200-140699000	Strong transcription	Esophagus	oesophagus
15	chr9:140668200-140700000	Strong transcription	Fetal Brain Female	brain
16	chr9:140675000-140689800	Weak transcription	Fetal Brain Male	brain
17	chr9:140675600-140690800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:140675600-140698600	Strong transcription	Placenta	Placenta
19	chr9:140675800-140688400	Strong transcription	Brain Germinal Matrix	brain
20	chr9:140675800-140695600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr9:140676000-140690800	Strong transcription	Primary T helper cells PMA-I stimulated	--
22	chr9:140676400-140699400	Weak transcription	Fetal Heart	heart
23	chr9:140677400-140689400	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr9:140678000-140687200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr9:140678400-140689600	Weak transcription	Small Intestine	intestine
26	chr9:140679600-140687200	Weak transcription	Fetal Lung	lung
27	chr9:140679600-140687400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr9:140679600-140700000	Strong transcription	Fetal Muscle Leg	muscle
29	chr9:140679600-140710200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr9:140680600-140700000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr9:140680800-140688000	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr9:140681000-140711400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr9:140681200-140686200	Strong transcription	NHLF	lung
34	chr9:140681200-140700000	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr9:140681200-140704400	Strong transcription	Fetal Muscle Trunk	muscle
36	chr9:140681200-140704600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr9:140681400-140698400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr9:140681400-140699200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr9:140681400-140699800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr9:140681400-140699800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr9:140681600-140700200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:140682000-140687000	Weak transcription	Brain Substantia Nigra	brain
43	chr9:140682200-140687000	Weak transcription	Brain Angular Gyrus	brain
44	chr9:140682400-140687400	Weak transcription	Brain Hippocampus Middle	brain
45	chr9:140682400-140699200	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr9:140683000-140696600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr9:140683000-140700200	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr9:140683600-140687600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr9:140683600-140698200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr9:140683600-140698400	Strong transcription	Primary T cells fromperipheralblood	blood

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