Variant report

Variant	nsv466435
Chromosome Location	chr9:94165889-94225537
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2257)
CpG islands
(count:1286)
Chromatin interactive
region (count:71)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2257 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:94181459-94182518	K562	blood:	n/a	n/a
2	ARID3A	chr9:94183963-94184155	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:94187337-94187649	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:94166254-94166412	K562	blood:	n/a	n/a
5	ARID3A	chr9:94188145-94188752	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:94184804-94185312	K562	blood:	n/a	n/a
7	ARID3A	chr9:94186776-94187086	HepG2	liver:	n/a	chr9:94186906-94186921
8	ARID3A	chr9:94195510-94195852	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:94186325-94186477	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:94182665-94183124	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:94186886-94187049	K562	blood:	n/a	chr9:94186906-94186921
12	ARID3A	chr9:94180626-94182452	HepG2	liver:	n/a	n/a
13	ATF1	chr9:94188537-94188851	K562	blood:	n/a	n/a
14	ATF1	chr9:94166227-94166484	K562	blood:	n/a	n/a
15	ATF1	chr9:94185171-94186314	K562	blood:	n/a	chr9:94185332-94185346 chr9:94185410-94185424
16	ATF1	chr9:94181514-94182145	K562	blood:	n/a	n/a
17	ATF2	chr9:94177530-94177954	GM12878	blood:	n/a	n/a
18	ATF2	chr9:94177539-94177983	GM12878	blood:	n/a	n/a
19	ATF3	chr9:94186011-94186204	K562	blood:	n/a	chr9:94186159-94186179
20	ATF3	chr9:94181321-94182266	HCT-116	colon:	n/a	n/a
21	ATF3	chr9:94195382-94195824	A549	lung:	n/a	n/a
22	ATF3	chr9:94181434-94181959	K562	blood:	n/a	n/a
23	BACH1	chr9:94185365-94185717	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr9:94184235-94184241	K562	blood:	n/a	n/a
25	BACH1	chr9:94186106-94186123	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr9:94185250-94185410	K562	blood:	n/a	n/a
27	BACH1	chr9:94183768-94184101	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr9:94186392-94187473	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr9:94166302-94166502	K562	blood:	n/a	n/a
30	BATF	chr9:94177541-94177963	GM12878	blood:	n/a	n/a
31	BATF	chr9:94177631-94177943	GM12878	blood:	n/a	n/a
32	BCL3	chr9:94181394-94181989	A549	lung:	n/a	n/a
33	BCL3	chr9:94195421-94195987	A549	lung:	n/a	n/a
34	BCLAF1	chr9:94177514-94177954	GM12878	blood:	n/a	n/a
35	BCLAF1	chr9:94177566-94177911	GM12878	blood:	n/a	n/a
36	BHLHE40	chr9:94166248-94166411	K562	blood:	n/a	n/a
37	BHLHE40	chr9:94181588-94182125	A549	lung:	n/a	n/a
38	BHLHE40	chr9:94181520-94182303	K562	blood:	n/a	n/a
39	BHLHE40	chr9:94177615-94177898	GM12878	blood:	n/a	n/a
40	BHLHE40	chr9:94181515-94182224	HepG2	liver:	n/a	n/a
41	BHLHE40	chr9:94208084-94208086	HepG2	liver:	n/a	n/a
42	BHLHE40	chr9:94186061-94187639	K562	blood:	n/a	chr9:94186850-94186866 chr9:94186987-94187003 chr9:94186778-94186794
43	BHLHE40	chr9:94185267-94185842	K562	blood:	n/a	chr9:94185780-94185796 chr9:94185646-94185662
44	BHLHE40	chr9:94186058-94187432	HepG2	liver:	n/a	chr9:94186850-94186866 chr9:94186987-94187003 chr9:94186778-94186794
45	BRCA1	chr9:94186810-94186944	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr9:94181426-94182525	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr9:94186453-94186536	HepG2	liver:	n/a	n/a
48	BRCA1	chr9:94186872-94187021	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr9:94184166-94185781	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr9:94195565-94195891	Hela-S3	cervix:	n/a	n/a

(count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:94186556-94186606	PrEC	prostate:	n/a
2	chr9:94187090-94187140	ProgFib	skin:	n/a
3	chr9:94187181-94187231	HCPEpiC	choroid plexus:	n/a
4	chr9:94179786-94179836	T-47D	breast:	n/a
5	chr9:94172975-94173025	HepG2	liver:	n/a
6	chr9:94186556-94186606	PrEC	prostate:	n/a
7	chr9:94187090-94187140	ProgFib	skin:	n/a
8	chr9:94187181-94187231	HCPEpiC	choroid plexus:	n/a
9	chr9:94179786-94179836	T-47D	breast:	n/a
10	chr9:94172975-94173025	HepG2	liver:	n/a
11	chr9:94168100-94168150	HPAEpiC	pulmonary alveolar:	n/a
12	chr9:94168100-94168150	PrEC	prostate:	n/a
13	chr9:94190932-94190982	HCM	heart:	n/a
14	chr9:94168100-94168150	GM06990	blood:	n/a
15	chr9:94186556-94186606	GM12892	blood:	n/a
16	chr9:94186148-94186198	HRCEpiC	kidney:	n/a
17	chr9:94187090-94187140	A549	lung:	n/a
18	chr9:94186148-94186198	U87	brain:	n/a
19	chr9:94185528-94185578	Caco-2	colon:	n/a
20	chr9:94181612-94181662	PFSK-1	brain:	n/a
21	chr9:94183343-94183393	HCM	heart:	n/a
22	chr9:94184131-94184181	LNCaP	prostate:	n/a
23	chr9:94183408-94183458	Hepatocyte	liver:	n/a
24	chr9:94183408-94183458	GM19239	blood:	n/a
25	chr9:94179786-94179836	HNPCEpiC	eye:	n/a
26	chr9:94182501-94182551	MCF10A-Er-Src	breast:	n/a
27	chr9:94187714-94187764	CMK	blood:	n/a
28	chr9:94186957-94187007	SAEC	small airway:	n/a
29	chr9:94178868-94178918	A549	lung:	n/a
30	chr9:94186148-94186198	HEK293	kidney:	embryo
31	chr9:94187714-94187764	HCPEpiC	choroid plexus:	n/a
32	chr9:94186556-94186606	ECC-1	luminal epithelium:	n/a
33	chr9:94183343-94183393	SAEC	small airway:	n/a
34	chr9:94187090-94187140	Jurkat	blood:	n/a
35	chr9:94183343-94183393	HepG2	liver:	n/a
36	chr9:94172975-94173025	Hela-S3	cervix:	n/a
37	chr9:94186148-94186198	AG10803	skin:	n/a
38	chr9:94184131-94184181	HCF	heart:	n/a
39	chr9:94185698-94185748	HUVEC	blood vessel:	n/a
40	chr9:94185528-94185578	ProgFib	skin:	n/a
41	chr9:94185786-94185836	NT2-D1	testis:	n/a
42	chr9:94186148-94186198	PrEC	prostate:	n/a
43	chr9:94187090-94187140	HEEpiC	esophagus:	n/a
44	chr9:94178868-94178918	GM12892	blood:	n/a
45	chr9:94172975-94173025	HEK293	kidney:	embryo
46	chr9:94184131-94184181	SKMC	muscle:	n/a
47	chr9:94181612-94181662	PANC-1	pancreas:	n/a
48	chr9:94190932-94190982	IMR90	lung:	fetal
49	chr9:94186148-94186198	SK-N-SH_RA	brain:	n/a
50	chr9:94172975-94173025	SAEC	small airway:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:94169920..94172701-chr9:94176209..94178713,2	MCF-7	breast:
2	chr9:94219655..94222504-chr9:94223136..94226019,2	K562	blood:
3	chr9:94159501..94162082-chr9:94181807..94183814,2	K562	blood:
4	chr9:94185231..94188165-chr9:94188188..94190328,4	MCF-7	breast:
5	chr9:93747219..93748073-chr9:94195149..94195713,2	MCF-7	breast:
6	chr9:93953851..93958747-chr9:94181568..94185373,5	K562	blood:
7	chr9:94117817..94120957-chr9:94180896..94184221,3	MCF-7	breast:
8	chr9:94122308..94125236-chr9:94184727..94188096,6	K562	blood:
9	chr9:94168114..94169747-chr9:94171117..94173856,2	K562	blood:
10	chr9:93955512..93957645-chr9:94181568..94183093,2	K562	blood:
11	chr9:93795748..93796306-chr9:94195154..94195880,2	K562	blood:
12	chr9:94123656..94126341-chr9:94180396..94182499,3	K562	blood:
13	chr3:169482224..169483207-chr9:94186851..94187807,2	Hela-S3	cervix:
14	chr9:94172287..94174445-chr9:94176873..94178600,2	K562	blood:
15	chr9:94167864..94173787-chr9:94174418..94178373,7	K562	blood:
16	chr9:94164043..94167657-chr9:94182944..94185733,4	K562	blood:
17	chr17:40425992..40426593-chr9:94186302..94186840,2	Hela-S3	cervix:
18	chr9:94159501..94162102-chr9:94181746..94183814,3	K562	blood:
19	chr9:94186298..94187810-chr9:94475229..94478202,2	MCF-7	breast:
20	chr9:94195123..94195732-chr9:94443735..94444600,2	MCF-7	breast:
21	chr9:93677291..93677869-chr9:94195160..94195912,2	MCF-7	breast:
22	chr9:94155980..94157529-chr9:94180110..94182915,2	K562	blood:
23	chr9:93851568..93852532-chr9:94195225..94195747,2	MCF-7	breast:
24	chr17:57914194..57917081-chr9:94185879..94187778,2	MCF-7	breast:
25	chr9:93723393..93725227-chr9:94195689..94197370,2	MCF-7	breast:
26	chr2:102313812..102314678-chr9:94185695..94186438,2	Hela-S3	cervix:
27	chr9:94185224..94187549-chr9:94194059..94196684,4	MCF-7	breast:
28	chr9:94203480..94205514-chr9:94206490..94208328,2	MCF-7	breast:
29	chr9:94172287..94174445-chr9:94176873..94178600,2	K562	blood:
30	chr9:94184878..94187918-chr9:94204912..94208983,3	K562	blood:
31	chr9:93957539..93960381-chr9:94183192..94185284,2	K562	blood:
32	chr9:94164043..94167657-chr9:94182944..94185733,4	K562	blood:
33	chr9:94183995..94185934-chr9:94211756..94213508,2	MCF-7	breast:
34	chr9:94219655..94222504-chr9:94223136..94226019,2	K562	blood:
35	chr9:94099269..94101700-chr9:94165480..94167430,2	K562	blood:
36	chr9:93957439..93960002-chr9:94175554..94177505,2	K562	blood:
37	chr9:94122021..94124488-chr9:94184872..94187456,5	MCF-7	breast:
38	chr9:94098360..94101047-chr9:94184402..94186027,2	MCF-7	breast:
39	chr9:94122646..94126004-chr9:94185203..94187645,6	MCF-7	breast:
40	chr9:93725779..93727886-chr9:94185947..94188539,2	MCF-7	breast:
41	chr9:93677407..93679291-chr9:94178811..94181688,2	MCF-7	breast:
42	chr9:94183995..94185934-chr9:94211756..94213508,2	MCF-7	breast:
43	chr9:94187794..94191937-chr9:94194042..94196809,3	MCF-7	breast:
44	chr9:94120989..94122585-chr9:94173872..94176280,2	K562	blood:
45	chr9:93921068..93922852-chr9:94184016..94186488,2	MCF-7	breast:
46	chr17:35766757..35767455-chr9:94185377..94186353,2	Hela-S3	cervix:
47	chr9:94120744..94125236-chr9:94184262..94187726,6	K562	blood:
48	chr9:94189299..94191359-chr9:94191598..94193415,2	MCF-7	breast:
49	chr17:72439167..72439675-chr9:94186282..94186911,2	Hela-S3	cervix:
50	chr9:94122194..94124570-chr9:94181630..94183264,3	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SYK-6	chr9:94188446-94188678	NONHSAT133136
2	lnc-SYK-6	chr9:94189112-94189429	XLOC_007456
3	lnc-SYK-6	chr9:94186604-94187534	XLOC_007456
4	lnc-SYK-10	chr9:94218804-94219352	predAs_ge08_OMD_2
5	lnc-SYK-6	chr9:94189112-94189408	NONHSAT133136
6	lnc-SYK-6	chr9:94188520-94188678	XLOC_007456
7	lnc-SYK-6	chr9:94189112-94189426	XLOC_007456

No data

Variant related genes	Relation type
NFIL3	TF binding region
ENSG00000233081	TF binding region
NFIL3	CpG island
ENSG00000233081	CpG island
ENSG00000170412	chromatin interactions
ENSG00000165030	chromatin interactions
ENSG00000148090	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000233081	chromatin interactions
ENSG00000071054	chromatin interactions
ENSG00000228216	chromatin interactions
ENSG00000108264	chromatin interactions
ENSG00000132142	chromatin interactions
ENSG00000235641	chromatin interactions
ENSG00000137409	chromatin interactions
ENSG00000270141	chromatin interactions
KIAA0240	miRNA target sites
TBC1D8B	miRNA target sites

Extended variants
information (count: 1614 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1614 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1758695	chr9:94165889-94165890	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs550677703	chr9:94165943-94165944	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs571161879	chr9:94165982-94165983	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs572132893	chr9:94165984-94165985	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs77049530	chr9:94166004-94166005	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs140205562	chr9:94166006-94166007	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs7021111	chr9:94166021-94166022	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs117301128	chr9:94166058-94166059	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs56108610	chr9:94166069-94166070	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs75456619	chr9:94166097-94166098	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs80090933	chr9:94166101-94166102	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs556041131	chr9:94166105-94166106	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs1663502	chr9:94166106-94166107	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs538562219	chr9:94166111-94166112	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs556594329	chr9:94166183-94166184	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs71990825	chr9:94166189-94166190	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs529816772	chr9:94166191-94166192	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs531817698	chr9:94166198-94166199	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs59763312	chr9:94166236-94166237	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs184115266	chr9:94166315-94166316	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs60422692	chr9:94166335-94166336	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs572642623	chr9:94166352-94166353	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs540036861	chr9:94166386-94166387	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs545536222	chr9:94166412-94166413	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs143536752	chr9:94166420-94166421	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs529136018	chr9:94166426-94166427	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs544464104	chr9:94166442-94166443	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs565046922	chr9:94166443-94166444	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs116698992	chr9:94166444-94166445	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs533313492	chr9:94166445-94166446	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs79584359	chr9:94166451-94166452	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs560563450	chr9:94166452-94166453	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs539469085	chr9:94166465-94166466	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs527813136	chr9:94166466-94166467	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs549580535	chr9:94166493-94166494	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs567825209	chr9:94166494-94166495	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs2440585	chr9:94166510-94166511	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs550402444	chr9:94166512-94166513	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs189366972	chr9:94166523-94166524	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs539410186	chr9:94166538-94166539	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs115567765	chr9:94166559-94166560	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs143177293	chr9:94166580-94166581	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs572582455	chr9:94166604-94166605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375836620	chr9:94166633-94166634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs13302545	chr9:94166693-94166694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533675901	chr9:94166733-94166734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555061465	chr9:94166734-94166735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573755624	chr9:94166735-94166736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs192211944	chr9:94166741-94166742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550669170	chr9:94166746-94166747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:1641 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94158000-94169800	Weak transcription	Liver	Liver
2	chr9:94158200-94168000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:94158200-94170000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr9:94158200-94171400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr9:94158200-94171800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr9:94158400-94171400	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr9:94158800-94167400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:94158800-94169000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:94158800-94169000	Weak transcription	NHDF-Ad	bronchial
10	chr9:94158800-94171800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr9:94159000-94167800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:94159000-94168800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:94159000-94168800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr9:94159000-94169000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr9:94159000-94169800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr9:94159000-94171400	Weak transcription	HUVEC	blood vessel
17	chr9:94159000-94171400	Weak transcription	NH-A	brain
18	chr9:94159200-94169000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr9:94159200-94169800	Weak transcription	Osteobl	bone
20	chr9:94159200-94170000	Weak transcription	NHLF	lung
21	chr9:94159200-94170200	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr9:94159200-94171400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr9:94159200-94171400	Weak transcription	HSMM	muscle
24	chr9:94159400-94166800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr9:94159400-94169800	Weak transcription	Placenta	Placenta
26	chr9:94161400-94170000	Weak transcription	Fetal Brain Female	brain
27	chr9:94161600-94170000	Weak transcription	Aorta	Aorta
28	chr9:94162000-94171400	Weak transcription	Fetal Brain Male	brain
29	chr9:94162400-94171800	Weak transcription	Spleen	Spleen
30	chr9:94162600-94169800	Weak transcription	Adipose Nuclei	Adipose
31	chr9:94162600-94171400	Weak transcription	Fetal Kidney	kidney
32	chr9:94163800-94170000	Weak transcription	Right Ventricle	heart
33	chr9:94164200-94172000	Weak transcription	Brain Germinal Matrix	brain
34	chr9:94164200-94181800	Weak transcription	Psoas Muscle	Psoas
35	chr9:94165000-94166600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr9:94165000-94168000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr9:94165200-94166000	Enhancers	K562	blood
38	chr9:94165200-94166600	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr9:94165200-94166600	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr9:94165200-94166800	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr9:94165400-94166000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr9:94165600-94166400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:94165600-94167800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr9:94165600-94170000	Weak transcription	Pancreas	Pancrea
45	chr9:94165600-94170200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr9:94165800-94166000	Enhancers	Primary hematopoietic stem cells	blood
47	chr9:94165800-94166000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr9:94165800-94166000	Enhancers	Brain Substantia Nigra	brain
49	chr9:94165800-94166000	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr9:94165800-94166400	Enhancers	Fetal Intestine Large	intestine

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