Variant report

Variant	nsv892573
Chromosome Location	chr9:12730636-12874703
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2385)
CpG islands
(count:307)
Chromatin interactive
region (count:94)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2385 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:12812740-12812885	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:12794096-12794882	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:12775950-12776944	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:12813647-12814934	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:12814233-12814684	K562	blood:	n/a	n/a
6	ARID3A	chr9:12784048-12785110	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:12816761-12818215	HepG2	liver:	n/a	chr9:12817708-12817724
8	ARID3A	chr9:12815975-12816358	HepG2	liver:	n/a	n/a
9	ATF1	chr9:12814215-12814687	K562	blood:	n/a	n/a
10	ATF2	chr9:12735567-12735964	GM12878	blood:	n/a	n/a
11	ATF2	chr9:12735544-12735972	GM12878	blood:	n/a	n/a
12	ATF3	chr9:12814080-12814958	HCT-116	colon:	n/a	n/a
13	ATF3	chr9:12776028-12776603	A549	lung:	n/a	n/a
14	ATF3	chr9:12814116-12814883	A549	lung:	n/a	n/a
15	ATF3	chr9:12784324-12785046	A549	lung:	n/a	n/a
16	ATF3	chr9:12814089-12814909	HCT-116	colon:	n/a	n/a
17	ATF3	chr9:12814140-12814884	A549	lung:	n/a	n/a
18	ATF3	chr9:12784352-12784992	A549	lung:	n/a	n/a
19	BACH1	chr9:12784589-12784652	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr9:12784537-12784775	K562	blood:	n/a	n/a
21	BACH1	chr9:12775963-12776675	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr9:12784440-12784836	GM12878	blood:	n/a	chr9:12784627-12784638
23	BATF	chr9:12784487-12784808	GM12878	blood:	n/a	chr9:12784627-12784638
24	BCL11A	chr9:12784486-12784786	GM12878	blood:	n/a	n/a
25	BCL3	chr9:12813964-12815230	A549	lung:	n/a	chr9:12814953-12814962
26	BCL3	chr9:12784221-12785015	A549	lung:	n/a	n/a
27	BCL3	chr9:12775887-12777064	A549	lung:	n/a	chr9:12776114-12776127
28	BCL3	chr9:12859624-12860315	A549	lung:	n/a	chr9:12859689-12859698
29	BCL3	chr9:12794096-12794785	A549	lung:	n/a	n/a
30	BCL3	chr9:12784331-12785068	A549	lung:	n/a	n/a
31	BCL3	chr9:12814100-12814872	A549	lung:	n/a	n/a
32	BCL3	chr9:12775944-12776770	A549	lung:	n/a	chr9:12776114-12776127
33	BCL3	chr9:12774751-12775592	A549	lung:	n/a	chr9:12775208-12775217
34	BHLHE40	chr9:12816828-12817176	HepG2	liver:	n/a	n/a
35	BHLHE40	chr9:12814145-12814857	A549	lung:	n/a	n/a
36	BHLHE40	chr9:12776058-12776346	HepG2	liver:	n/a	n/a
37	BHLHE40	chr9:12784391-12784791	K562	blood:	n/a	n/a
38	BHLHE40	chr9:12814481-12814829	K562	blood:	n/a	n/a
39	BHLHE40	chr9:12784559-12784788	GM12878	blood:	n/a	n/a
40	BHLHE40	chr9:12814024-12814857	HepG2	liver:	n/a	n/a
41	BHLHE40	chr9:12776329-12776638	K562	blood:	n/a	n/a
42	BHLHE40	chr9:12827183-12827244	A549	lung:	n/a	n/a
43	BHLHE40	chr9:12816834-12817221	HepG2	liver:	n/a	n/a
44	BHLHE40	chr9:12771808-12772164	A549	lung:	n/a	n/a
45	BHLHE40	chr9:12775478-12776767	HepG2	liver:	n/a	chr9:12775512-12775528 chr9:12776042-12776058
46	BHLHE40	chr9:12776015-12776514	GM12878	blood:	n/a	chr9:12776042-12776058
47	BHLHE40	chr9:12784373-12785060	HepG2	liver:	n/a	n/a
48	BRCA1	chr9:12784182-12784865	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr9:12776070-12777883	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr9:12776076-12776725	HepG2	liver:	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	chr9:12774985-12775035	HIPEpiC	eye:	n/a
2	chr9:12775700-12775750	BJ	skin:	n/a
3	chr9:12774985-12775035	HIPEpiC	eye:	n/a
4	chr9:12775700-12775750	BJ	skin:	n/a
5	chr9:12775750-12775800	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:12775750-12775800	AG09319	gingival:	n/a
7	chr9:12775700-12775750	PANC-1	pancreas:	n/a
8	chr9:12775750-12775800	HCM	heart:	n/a
9	chr9:12776046-12776096	AG09319	gingival:	n/a
10	chr9:12774985-12775035	SK-N-SH_RA	brain:	n/a
11	chr9:12774985-12775035	HUVEC	blood vessel:	n/a
12	chr9:12776218-12776268	SAEC	small airway:	n/a
13	chr9:12775750-12775800	SK-N-SH	brain:	n/a
14	chr9:12775700-12775750	GM19239	blood:	n/a
15	chr9:12775750-12775800	NHBE	bronchial:	n/a
16	chr9:12776218-12776268	AG09319	gingival:	n/a
17	chr9:12776046-12776096	IMR90	lung:	fetal
18	chr9:12774985-12775035	HEEpiC	esophagus:	n/a
19	chr9:12775700-12775750	NT2-D1	testis:	n/a
20	chr9:12776218-12776268	HRE	kidney:	n/a
21	chr9:12776046-12776096	AoSMC	blood vessel:	n/a
22	chr9:12774985-12775035	AG09319	gingival:	n/a
23	chr9:12774985-12775035	SAEC	small airway:	n/a
24	chr9:12774985-12775035	AG10803	skin:	n/a
25	chr9:12776218-12776268	ECC-1	luminal epithelium:	n/a
26	chr9:12775750-12775800	BJ	skin:	n/a
27	chr9:12776046-12776096	SK-N-MC	brain:	n/a
28	chr9:12776218-12776268	GM06990	blood:	n/a
29	chr9:12776218-12776268	Hepatocyte	liver:	n/a
30	chr9:12776046-12776096	BE2_C	brain:	n/a
31	chr9:12775700-12775750	HRCEpiC	kidney:	n/a
32	chr9:12776046-12776096	ECC-1	luminal epithelium:	n/a
33	chr9:12776218-12776268	BJ	skin:	n/a
34	chr9:12776046-12776096	HCF	heart:	n/a
35	chr9:12775750-12775800	SK-N-MC	brain:	n/a
36	chr9:12776218-12776268	NHDF-neo	bronchial:	n/a
37	chr9:12775700-12775750	HCT-116	colon:	n/a
38	chr9:12776046-12776096	RPTEC	kidney:	n/a
39	chr9:12775700-12775750	T-47D	breast:	n/a
40	chr9:12774985-12775035	HCPEpiC	choroid plexus:	n/a
41	chr9:12774985-12775035	Caco-2	colon:	n/a
42	chr9:12775750-12775800	HepG2	liver:	n/a
43	chr9:12775700-12775750	HepG2	liver:	n/a
44	chr9:12775700-12775750	GM06990	blood:	n/a
45	chr9:12775700-12775750	K562	blood:	n/a
46	chr9:12774985-12775035	CMK	blood:	n/a
47	chr9:12776218-12776268	HepG2	liver:	n/a
48	chr9:12775700-12775750	AG04450	lung:	fetal
49	chr9:12776046-12776096	AG04449	skin:	fetal
50	chr9:12776046-12776096	A549	lung:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:12815854..12818984-chr9:12830927..12834079,3	MCF-7	breast:
2	chr9:12774993..12776787-chr9:12859999..12861752,2	MCF-7	breast:
3	chr9:12788809..12790728-chr9:12792217..12794767,4	MCF-7	breast:
4	chr9:12794123..12798425-chr9:12799018..12802796,5	MCF-7	breast:
5	chr9:12774105..12776446-chr9:12796570..12799387,2	MCF-7	breast:
6	chr9:12786137..12788108-chr9:12801967..12804015,2	MCF-7	breast:
7	chr9:12732393..12734244-chr9:12774652..12776497,2	MCF-7	breast:
8	chr9:12783262..12785196-chr9:12857512..12860310,2	MCF-7	breast:
9	chr9:12775994..12778011-chr9:12786037..12787743,2	K562	blood:
10	chr9:12785493..12787579-chr9:12811391..12813312,2	MCF-7	breast:
11	chr9:12773969..12780098-chr9:12789328..12796142,13	MCF-7	breast:
12	chr9:12773433..12781932-chr9:12782481..12798090,47	MCF-7	breast:
13	chr9:12851201..12854512-chr9:12857301..12860029,3	MCF-7	breast:
14	chr9:5854256..5856803-chr9:12790614..12793175,2	MCF-7	breast:
15	chr9:12774525..12776496-chr9:12779870..12781458,2	MCF-7	breast:
16	chr9:12816957..12819670-chr9:12821766..12823551,2	MCF-7	breast:
17	chr9:12816711..12819917-chr9:12821131..12823680,3	MCF-7	breast:
18	chr9:12851201..12854512-chr9:12857301..12860029,3	MCF-7	breast:
19	chr9:12776384..12777092-chr9:12988313..12988856,2	MCF-7	breast:
20	chr9:12784133..12787098-chr9:12813508..12817370,4	MCF-7	breast:
21	chr9:12779288..12781566-chr9:12835012..12836710,2	MCF-7	breast:
22	chr9:12778616..12780365-chr9:12854007..12856066,2	MCF-7	breast:
23	chr9:12776291..12778540-chr9:12858744..12861808,3	MCF-7	breast:
24	chr9:12786137..12788108-chr9:12801967..12804015,2	MCF-7	breast:
25	chr9:12791617..12793320-chr9:12793855..12796172,2	MCF-7	breast:
26	chr9:12788809..12790728-chr9:12792217..12794767,4	MCF-7	breast:
27	chr9:12775140..12777800-chr9:12796207..12799105,2	K562	blood:
28	chr9:12733476..12735004-chr9:12774992..12776567,2	MCF-7	breast:
29	chr9:12783262..12785196-chr9:12857512..12860310,2	MCF-7	breast:
30	chr9:12833643..12836403-chr9:12844199..12845787,2	MCF-7	breast:
31	chr9:12827106..12828811-chr9:12846763..12849036,2	MCF-7	breast:
32	chr9:12784573..12785102-chr9:12794160..12794796,2	MCF-7	breast:
33	chr9:12774903..12777791-chr9:12804200..12806212,3	MCF-7	breast:
34	chr9:12796888..12798629-chr9:12811320..12813907,2	MCF-7	breast:
35	chr9:12776937..12779598-chr9:12883479..12885184,2	MCF-7	breast:
36	chr9:12774887..12777356-chr9:12828580..12830955,2	MCF-7	breast:
37	chr3:21274702..21276486-chr9:12852043..12854335,2	MCF-7	breast:
38	chr9:12752690..12755433-chr9:12775370..12778156,2	MCF-7	breast:
39	chr9:12833643..12836403-chr9:12844199..12845787,2	MCF-7	breast:
40	chr9:12773974..12784053-chr9:12813051..12820453,19	MCF-7	breast:
41	chr9:12810284..12814602-chr9:12816113..12819154,5	MCF-7	breast:
42	chr9:12789292..12791495-chr9:12794969..12797067,2	MCF-7	breast:
43	chr9:12774319..12775976-chr9:12801872..12803906,2	MCF-7	breast:
44	chr9:12774109..12791345-chr9:12812800..12822770,37	MCF-7	breast:
45	chr9:12750217..12752763-chr9:12757622..12759170,2	MCF-7	breast:
46	chr9:12796888..12798629-chr9:12811320..12813907,2	MCF-7	breast:
47	chr9:12794502..12796197-chr9:13084693..13086368,2	MCF-7	breast:
48	chr9:12777697..12781582-chr9:12805623..12809956,4	MCF-7	breast:
49	chr9:12827106..12828811-chr9:12846763..12849036,2	MCF-7	breast:
50	chr9:12777697..12781582-chr9:12805623..12809956,4	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPDZ-1	chr9:12814292-12814344	ENSG00000235448.1
2	lnc-MPDZ-1	chr9:12759551-12759623	ENSG00000235448.1
3	lnc-C9orf150-2	chr9:12758922-12759300	l_3734_chr9:12728518-12759537_heart
4	lnc-C9orf150-1	chr9:12768922-12770158	XLOC_007283
5	lnc-MPDZ-8	chr9:12764762-12765054	NONHSAT130228
6	lnc-C9orf150-1	chr9:12738519-12738662	XLOC_007283
7	lnc-MPDZ-1	chr9:12790619-12790764	ENSG00000235448.1
8	lnc-C9orf150-2	chr9:12759301-12759537	l_3734_chr9:12728518-12759537_heart

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C9orf150	hsa-miR-335-5p	chr9:12822120-12822143

Variant related genes	Relation type
RN7SL849P	TF binding region
LURAP1L	TF binding region
ENSG00000235448	TF binding region
RN7SL849P	CpG island
LURAP1L	CpG island
ENSG00000235448	CpG island
ENSG00000261393	chromatin interactions
ENSG00000223621	chromatin interactions
ENSG00000235448	chromatin interactions
ENSG00000166164	chromatin interactions
ENSG00000178904	chromatin interactions
ENSG00000222658	chromatin interactions
ENSG00000269093	chromatin interactions
ENSG00000153714	chromatin interactions
ENSG00000267213	chromatin interactions

Extended variants
information (count: 7140 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:7140 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7025758	chr9:12730636-12730637	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185711589	chr9:12730648-12730649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532364773	chr9:12730653-12730654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552114619	chr9:12730663-12730664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113217039	chr9:12730675-12730676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569341132	chr9:12730709-12730710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375813917	chr9:12730733-12730734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149902670	chr9:12730740-12730741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528450191	chr9:12730748-12730749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548795704	chr9:12730750-12730751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144966898	chr9:12730762-12730763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140648759	chr9:12730770-12730771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7026199	chr9:12730800-12730801	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs577567388	chr9:12730827-12730828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565032566	chr9:12730831-12730832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372443962	chr9:12730834-12730835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539451183	chr9:12730866-12730867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536005581	chr9:12730870-12730871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188838604	chr9:12730876-12730877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145812446	chr9:12730885-12730886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138456346	chr9:12730886-12730887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577184236	chr9:12730906-12730907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7026121	chr9:12730924-12730925	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs572136158	chr9:12730990-12730991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12001737	chr9:12731068-12731069	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs10960766	chr9:12731082-12731083	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs180804303	chr9:12731092-12731093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558514682	chr9:12731140-12731141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529920324	chr9:12731141-12731142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546544623	chr9:12731213-12731214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533015367	chr9:12731214-12731215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552178009	chr9:12731243-12731244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10960767	chr9:12731261-12731262	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs185429086	chr9:12731290-12731291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548386127	chr9:12731312-12731313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568685764	chr9:12731329-12731330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116362477	chr9:12731342-12731343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10756398	chr9:12731343-12731344	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs10960768	chr9:12731367-12731368	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs568967085	chr9:12731390-12731391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556151106	chr9:12731399-12731400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191872540	chr9:12731465-12731466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373936644	chr9:12731493-12731494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535576104	chr9:12731542-12731543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537506050	chr9:12731581-12731582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141431002	chr9:12731589-12731590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571759745	chr9:12731595-12731596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540834099	chr9:12731609-12731610	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs563901208	chr9:12731613-12731614	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs574126248	chr9:12731623-12731624	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Disorders of sex development	21048976	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:2028 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12719200-12740400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:12729600-12731600	Enhancers	Fetal Lung	lung
3	chr9:12730400-12730800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:12730400-12731000	Enhancers	HUVEC	blood vessel
5	chr9:12731600-12732000	Flanking Active TSS	Fetal Lung	lung
6	chr9:12732000-12732600	Enhancers	Fetal Lung	lung
7	chr9:12732600-12736000	Weak transcription	Fetal Lung	lung
8	chr9:12734800-12736800	Enhancers	GM12878-XiMat	blood
9	chr9:12736000-12736200	Enhancers	Fetal Lung	lung
10	chr9:12736200-12737400	Weak transcription	Fetal Lung	lung
11	chr9:12737400-12739200	Enhancers	Fetal Lung	lung
12	chr9:12737400-12739400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:12737600-12737800	Enhancers	Fetal Muscle Leg	muscle
14	chr9:12737600-12738400	Enhancers	HSMMtube	muscle
15	chr9:12737600-12741000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:12737800-12738000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr9:12737800-12739400	Enhancers	NHDF-Ad	bronchial
18	chr9:12737800-12741200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:12738000-12738600	Enhancers	Fetal Kidney	kidney
20	chr9:12738000-12738800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr9:12738400-12738600	Enhancers	Fetal Muscle Leg	muscle
22	chr9:12738600-12739600	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr9:12738800-12739600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr9:12739000-12739200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr9:12739000-12739400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr9:12739000-12739600	Enhancers	Osteobl	bone
27	chr9:12739000-12741200	Enhancers	HMEC	breast
28	chr9:12739200-12739400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr9:12739200-12739600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr9:12739200-12739600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr9:12739200-12739600	Enhancers	Fetal Intestine Small	intestine
32	chr9:12739200-12740200	Weak transcription	Fetal Lung	lung
33	chr9:12739200-12741000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr9:12739200-12741400	Enhancers	NHEK	skin
35	chr9:12739400-12740000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr9:12739400-12740800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:12739600-12740000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr9:12739600-12740600	Weak transcription	Osteobl	bone
39	chr9:12739600-12740800	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr9:12740000-12741000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr9:12740000-12741400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr9:12740200-12740400	Enhancers	Fetal Lung	lung
43	chr9:12740400-12741600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr9:12740600-12741200	Enhancers	Osteobl	bone
45	chr9:12740800-12741200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr9:12740800-12741200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr9:12741000-12741200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr9:12741000-12741400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr9:12741400-12748400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr9:12741600-12747800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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