Variant report

Variant	nsv471309
Chromosome Location	chr9:72273898-72410323
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1747)
CpG islands
(count:794)
Chromatin interactive
region (count:89)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1747 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:72287778-72288055	HepG2	liver:	n/a	chr9:72287860-72287868
2	ARID3A	chr9:72361797-72362287	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:72373360-72373563	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:72374662-72375390	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:72367593-72367788	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:72363143-72363934	HepG2	liver:	n/a	n/a
7	ATF1	chr9:72342985-72343073	K562	blood:	n/a	n/a
8	ATF2	chr9:72287724-72288162	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr9:72374581-72375322	GM12878	blood:	n/a	n/a
10	ATF2	chr9:72374612-72374898	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr9:72287881-72288378	A549	lung:	n/a	n/a
12	BACH1	chr9:72408765-72408800	K562	blood:	n/a	n/a
13	BACH1	chr9:72386875-72387222	K562	blood:	n/a	n/a
14	BACH1	chr9:72374810-72375429	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:72361184-72361431	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:72287312-72288183	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr9:72386930-72387304	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr9:72374554-72374995	GM12878	blood:	n/a	chr9:72374713-72374726 chr9:72374600-72374613 chr9:72374747-72374756 chr9:72374896-72374909
19	BCL3	chr9:72374941-72375380	A549	lung:	n/a	chr9:72374995-72375004 chr9:72375362-72375371
20	BCLAF1	chr9:72374362-72375253	GM12878	blood:	n/a	chr9:72374713-72374726 chr9:72374995-72375004 chr9:72374600-72374613 chr9:72374747-72374756 chr9:72374896-72374909
21	BCLAF1	chr9:72374438-72375400	GM12878	blood:	n/a	chr9:72374713-72374726 chr9:72374995-72375004 chr9:72375362-72375371 chr9:72374600-72374613 chr9:72374747-72374756 chr9:72374896-72374909
22	BCLAF1	chr9:72287701-72288096	GM12878	blood:	n/a	chr9:72287806-72287819
23	BHLHE40	chr9:72374558-72375184	K562	blood:	n/a	chr9:72374717-72374733
24	BHLHE40	chr9:72373912-72375320	GM12878	blood:	n/a	chr9:72374717-72374733
25	BHLHE40	chr9:72287817-72288069	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:72287749-72288045	K562	blood:	n/a	n/a
27	BRCA1	chr9:72287860-72288060	HepG2	liver:	n/a	n/a
28	BRCA1	chr9:72374717-72374902	GM12878	blood:	n/a	n/a
29	BRCA1	chr9:72374762-72375287	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr9:72374817-72374948	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr9:72311799-72312056	K562	blood:	n/a	n/a
32	CBX3	chr9:72374715-72375218	K562	blood:	n/a	n/a
33	CBX3	chr9:72311776-72311985	K562	blood:	n/a	n/a
34	CCNT2	chr9:72334300-72334554	K562	blood:	n/a	n/a
35	CCNT2	chr9:72374533-72375194	K562	blood:	n/a	chr9:72374713-72374722
36	CCNT2	chr9:72365489-72365689	K562	blood:	n/a	n/a
37	CCNT2	chr9:72356512-72356681	K562	blood:	n/a	n/a
38	CEBPB	chr9:72374270-72375149	Hela-S3	cervix:	n/a	chr9:72375125-72375137
39	CEBPB	chr9:72355822-72356147	Hela-S3	cervix:	n/a	chr9:72355975-72355986
40	CEBPB	chr9:72369471-72369614	K562	blood:	n/a	n/a
41	CEBPB	chr9:72370248-72370532	HepG2	liver:	n/a	chr9:72370261-72370269
42	CEBPB	chr9:72355793-72356174	IMR90	lung:	n/a	chr9:72355975-72355986
43	CEBPB	chr9:72404742-72404801	HepG2	liver:	n/a	chr9:72404764-72404777 chr9:72404765-72404776 chr9:72404764-72404777
44	CEBPB	chr9:72342677-72342992	IMR90	lung:	n/a	n/a
45	CEBPB	chr9:72314796-72314959	HepG2	liver:	n/a	chr9:72314916-72314929
46	CEBPB	chr9:72334464-72334752	IMR90	lung:	n/a	n/a
47	CEBPB	chr9:72373047-72373391	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:72383612-72383912	IMR90	lung:	n/a	n/a
49	CEBPB	chr9:72332520-72332807	IMR90	lung:	n/a	n/a
50	CEBPB	chr9:72355869-72356090	A549	lung:	n/a	chr9:72355975-72355986

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:72288179-72288229	MCF-7	breast:	n/a
2	chr9:72288179-72288229	MCF-7	breast:	n/a
3	chr9:72288179-72288229	HepG2	liver:	n/a
4	chr9:72287772-72287822	HCM	heart:	n/a
5	chr9:72285588-72285638	SAEC	small airway:	n/a
6	chr9:72287772-72287822	MCF-7	breast:	n/a
7	chr9:72375599-72375649	BE2_C	brain:	n/a
8	chr9:72288098-72288148	PrEC	prostate:	n/a
9	chr9:72374488-72374538	CMK	blood:	n/a
10	chr9:72285588-72285638	HIPEpiC	eye:	n/a
11	chr9:72288156-72288206	HRE	kidney:	n/a
12	chr9:72374488-72374538	GM12892	blood:	n/a
13	chr9:72287772-72287822	IMR90	lung:	fetal
14	chr9:72288069-72288119	A549	lung:	n/a
15	chr9:72288179-72288229	NT2-D1	testis:	n/a
16	chr9:72288098-72288148	HRE	kidney:	n/a
17	chr9:72287152-72287202	SAEC	small airway:	n/a
18	chr9:72288179-72288229	GM19239	blood:	n/a
19	chr9:72287123-72287173	HCF	heart:	n/a
20	chr9:72374488-72374538	HCM	heart:	n/a
21	chr9:72374488-72374538	IMR90	lung:	fetal
22	chr9:72288069-72288119	BE2_C	brain:	n/a
23	chr9:72287772-72287822	MCF10A-Er-Src	breast:	n/a
24	chr9:72375599-72375649	HepG2	liver:	n/a
25	chr9:72287821-72287871	AG09319	gingival:	n/a
26	chr9:72287821-72287871	H1-hESC	embryonic stem cell:	embryo
27	chr9:72288098-72288148	HepG2	liver:	n/a
28	chr9:72287821-72287871	K562	blood:	n/a
29	chr9:72287152-72287202	HAEpiC	amniotic membrane:	n/a
30	chr9:72287821-72287871	HCT-116	colon:	n/a
31	chr9:72288156-72288206	HepG2	liver:	n/a
32	chr9:72287772-72287822	AG04450	lung:	fetal
33	chr9:72288179-72288229	A549	lung:	n/a
34	chr9:72285588-72285638	HepG2	liver:	n/a
35	chr9:72288069-72288119	CMK	blood:	n/a
36	chr9:72285588-72285638	T-47D	breast:	n/a
37	chr9:72288179-72288229	ProgFib	skin:	n/a
38	chr9:72371073-72371123	HCPEpiC	choroid plexus:	n/a
39	chr9:72288098-72288148	NB4	blood:	n/a
40	chr9:72287772-72287822	HRPEpiC	eye:	n/a
41	chr9:72288156-72288206	MCF-7	breast:	n/a
42	chr9:72288069-72288119	SK-N-MC	brain:	n/a
43	chr9:72287123-72287173	AG09319	gingival:	n/a
44	chr9:72288156-72288206	BJ	skin:	n/a
45	chr9:72288179-72288229	PFSK-1	brain:	n/a
46	chr9:72287772-72287822	HRCEpiC	kidney:	n/a
47	chr9:72287821-72287871	SK-N-SH_RA	brain:	n/a
48	chr9:72287821-72287871	NB4	blood:	n/a
49	chr9:72288179-72288229	GM12892	blood:	n/a
50	chr9:72371073-72371123	T-47D	breast:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:72360152..72362800-chr9:72364655..72369107,4	K562	blood:
2	chr9:72375036..72375536-chr9:73035083..73036042,2	Hela-S3	cervix:
3	chr9:72366292..72369666-chr9:72369993..72373484,7	K562	blood:
4	chr9:72286201..72287971-chr9:72360095..72361896,2	K562	blood:
5	chr9:72271323..72273681-chr9:72274273..72277521,4	K562	blood:
6	chr9:72363023..72365111-chr9:72369370..72372154,2	K562	blood:
7	chr9:72326559..72328464-chr9:72330242..72332864,2	K562	blood:
8	chr9:72373387..72376208-chr9:72873924..72875696,2	K562	blood:
9	chr9:72375672..72377949-chr9:72385605..72387785,2	K562	blood:
10	chr9:72351018..72353363-chr9:72366792..72368654,2	K562	blood:
11	chr9:72322031..72323753-chr9:72324057..72326681,2	MCF-7	breast:
12	chr9:72301601..72303893-chr9:72305400..72306910,2	MCF-7	breast:
13	chr9:72265675..72268152-chr9:72283798..72286751,2	MCF-7	breast:
14	chr9:72360858..72363722-chr9:72367124..72369107,2	K562	blood:
15	chr9:72364400..72366683-chr9:72367530..72370078,2	MCF-7	breast:
16	chr9:72375078..72376578-chr9:72378308..72381037,2	K562	blood:
17	chr9:72286195..72289118-chr9:72373474..72376010,3	MCF-7	breast:
18	chr1:156698163..156698747-chr9:72374771..72375332,2	Hela-S3	cervix:
19	chr9:72359106..72363474-chr9:72372322..72376083,7	MCF-7	breast:
20	chr9:72369892..72372039-chr9:72377603..72379852,2	MCF-7	breast:
21	chr9:72313523..72315444-chr9:72367244..72369414,2	K562	blood:
22	chr9:72351018..72353363-chr9:72366792..72368654,2	K562	blood:
23	chr9:72408903..72410772-chr9:72420063..72421971,2	K562	blood:
24	chr9:72357421..72360340-chr9:72369616..72371196,2	K562	blood:
25	chr9:72375011..72377307-chr9:72377548..72379098,2	K562	blood:
26	chr9:72259190..72261738-chr9:72289104..72291957,2	MCF-7	breast:
27	chr9:72399869..72402528-chr9:72404405..72407198,3	K562	blood:
28	chr9:72089279..72091764-chr9:72373318..72374835,2	MCF-7	breast:
29	chr9:72375765..72377296-chr9:72428952..72430591,2	K562	blood:
30	chr9:72361796..72363677-chr9:72418688..72421431,2	K562	blood:
31	chr9:72333686..72336207-chr9:72345738..72347762,3	K562	blood:
32	chr9:72364400..72366683-chr9:72367530..72370078,2	MCF-7	breast:
33	chr9:72375011..72377307-chr9:72377548..72379098,2	K562	blood:
34	chr9:72360748..72362784-chr9:72371625..72375303,3	K562	blood:
35	chr9:72360551..72362642-chr9:72371189..72374048,2	K562	blood:
36	chr9:72384593..72386711-chr9:72390096..72392732,2	K562	blood:
37	chr9:72366292..72369666-chr9:72369993..72373484,7	K562	blood:
38	chr9:72316586..72319182-chr9:72326502..72329352,2	K562	blood:
39	chr9:72333686..72336207-chr9:72345738..72347762,3	K562	blood:
40	chr9:72369991..72372114-chr9:72372371..72373981,2	K562	blood:
41	chr9:72360152..72362800-chr9:72364655..72369107,4	K562	blood:
42	chr9:72360551..72362642-chr9:72371189..72374048,2	K562	blood:
43	chr9:72316586..72319182-chr9:72326502..72329352,2	K562	blood:
44	chr9:72375017..72376522-chr9:72378625..72381142,2	MCF-7	breast:
45	chr9:72381383..72383690-chr9:72387681..72389643,2	K562	blood:
46	chr9:72287564..72288433-chr9:72400387..72401338,3	MCF-7	breast:
47	chr9:72371967..72374601-chr9:72378093..72381020,2	K562	blood:
48	chr9:72363859..72367648-chr9:72373327..72375290,5	MCF-7	breast:
49	chr9:72373340..72376294-chr9:72388394..72390368,2	K562	blood:
50	chr9:72384593..72387645-chr9:72389728..72392732,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf135-1	chr9:72408959-72409255	XLOC_007393
2	lnc-C9orf135-1	chr9:72402048-72402118	XLOC_007393
3	lnc-C9orf135-2	chr9:72287665-72288629	ENSG00000261447.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTAR1	hsa-miR-7-5p	chr9:72324647-72324640

Variant related genes	Relation type
PTAR1	TF binding region
APBA1	TF binding region
ENSG00000261447	TF binding region
PTAR1	CpG island
APBA1	CpG island
ENSG00000261447	CpG island
ENSG00000143303	chromatin interactions
ENSG00000185065	chromatin interactions
ENSG00000261447	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000107282	chromatin interactions
ENSG00000100084	chromatin interactions
ENSG00000198887	chromatin interactions
ENSG00000242259	chromatin interactions
ENSG00000127554	chromatin interactions
ENSG00000188647	chromatin interactions

Extended variants
information (count: 3734 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3734 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11139651	chr9:72273898-72273899	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529991612	chr9:72273957-72273958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542217439	chr9:72273968-72273969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563596904	chr9:72274053-72274054	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs374863985	chr9:72274218-72274219	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs531013040	chr9:72274238-72274239	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs539388183	chr9:72274253-72274254	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs148675736	chr9:72274289-72274290	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs528339860	chr9:72274309-72274310	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs546868417	chr9:72274326-72274327	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs549537006	chr9:72274374-72274375	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs75561828	chr9:72274380-72274381	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs185871131	chr9:72274447-72274448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568791784	chr9:72274634-72274635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539506212	chr9:72274644-72274645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189790826	chr9:72274649-72274650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557473696	chr9:72274677-72274678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182407560	chr9:72274682-72274683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142165660	chr9:72274686-72274687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187662439	chr9:72274782-72274783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533125763	chr9:72274824-72274825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73453583	chr9:72274874-72274875	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs34695133	chr9:72274999-72275000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541830095	chr9:72275051-72275052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566918880	chr9:72275091-72275092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563685335	chr9:72275116-72275117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs79146521	chr9:72275152-72275153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546275118	chr9:72275164-72275165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564572429	chr9:72275203-72275204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192141535	chr9:72275231-72275232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535712949	chr9:72275316-72275317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151064536	chr9:72275416-72275417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35776844	chr9:72275417-72275418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572261498	chr9:72275428-72275429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549552606	chr9:72275440-72275441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140969264	chr9:72275456-72275457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534898546	chr9:72275474-72275475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550637429	chr9:72275480-72275481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183910175	chr9:72275523-72275524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539110562	chr9:72275529-72275530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs72719102	chr9:72275565-72275566	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs188465095	chr9:72275580-72275581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566239278	chr9:72275619-72275620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575873475	chr9:72275660-72275661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534856332	chr9:72275674-72275675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553172453	chr9:72275676-72275677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574967943	chr9:72275693-72275694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536136625	chr9:72275697-72275698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77231473	chr9:72275744-72275745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149776361	chr9:72275748-72275749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
Melanoma	22183965	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	21811512	CNVD
Autism	21484199	CNVD
Breast cancer	22737080	CNVD
Malignant peripheral nerve sheath tumor	22811580	CNVD
Leprosy	22719964	CNVD
Primary ovarian insufficiency	22879975	CNVD
Glioma	20126413	CNVD
Malignant melanoma	17260012	CNVD

Chromatin state (count:3075 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72253000-72285000	Weak transcription	Fetal Brain Female	brain
2	chr9:72253400-72274400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:72258200-72274000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:72260600-72286200	Weak transcription	Aorta	Aorta
5	chr9:72262400-72274200	Weak transcription	Brain Angular Gyrus	brain
6	chr9:72262600-72285400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr9:72262800-72275600	Weak transcription	Brain Hippocampus Middle	brain
8	chr9:72264600-72275200	Weak transcription	Fetal Stomach	stomach
9	chr9:72269000-72274000	Weak transcription	Ovary	ovary
10	chr9:72272200-72276400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr9:72272600-72276000	Enhancers	Liver	Liver
12	chr9:72273000-72285600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:72273800-72274600	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr9:72273800-72275600	Enhancers	Fetal Lung	lung
15	chr9:72273800-72282600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:72274000-72274200	Bivalent Enhancer	Fetal Intestine Large	intestine
17	chr9:72274000-72274400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr9:72274000-72274400	Active TSS	Fetal Brain Male	brain
19	chr9:72274000-72274600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr9:72274000-72274600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr9:72274000-72274600	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr9:72274000-72274600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr9:72274000-72274600	Enhancers	Brain Anterior Caudate	brain
24	chr9:72274000-72274600	Enhancers	Fetal Kidney	kidney
25	chr9:72274000-72274800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr9:72274000-72274800	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr9:72274000-72274800	Enhancers	Ovary	ovary
28	chr9:72274000-72275400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:72274000-72275800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr9:72274200-72274600	Enhancers	Brain Angular Gyrus	brain
31	chr9:72274400-72274600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr9:72274400-72275600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr9:72274600-72276000	Weak transcription	Fetal Kidney	kidney
34	chr9:72274600-72278000	Weak transcription	Brain Angular Gyrus	brain
35	chr9:72274600-72280000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr9:72274600-72282000	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr9:72274600-72282200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr9:72274800-72275200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr9:72274800-72275200	Weak transcription	Ovary	ovary
40	chr9:72274800-72278800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr9:72275000-72276600	Enhancers	HUVEC	blood vessel
42	chr9:72275200-72275400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr9:72275200-72275400	Enhancers	Fetal Stomach	stomach
44	chr9:72275200-72275400	Enhancers	Ovary	ovary
45	chr9:72275200-72275600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr9:72275200-72275800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr9:72275200-72276000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr9:72275200-72276000	Enhancers	NH-A	brain
49	chr9:72275400-72276400	Weak transcription	Ovary	ovary
50	chr9:72275400-72278800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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