Variant report

Variant	nsv1030835
Chromosome Location	chr9:12717405-12840928
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2706)
CpG islands
(count:305)
Chromatin interactive
region (count:91)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2706 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:12814233-12814684	K562	blood:	n/a	n/a
2	ARID3A	chr9:12815975-12816358	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:12719466-12719806	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:12775950-12776944	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:12813647-12814934	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:12794096-12794882	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:12784048-12785110	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:12812740-12812885	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:12816761-12818215	HepG2	liver:	n/a	chr9:12817708-12817724
10	ATF1	chr9:12814215-12814687	K562	blood:	n/a	n/a
11	ATF2	chr9:12735544-12735972	GM12878	blood:	n/a	n/a
12	ATF2	chr9:12735567-12735964	GM12878	blood:	n/a	n/a
13	ATF3	chr9:12814140-12814884	A549	lung:	n/a	n/a
14	ATF3	chr9:12814116-12814883	A549	lung:	n/a	n/a
15	ATF3	chr9:12776028-12776603	A549	lung:	n/a	n/a
16	ATF3	chr9:12784324-12785046	A549	lung:	n/a	n/a
17	ATF3	chr9:12784352-12784992	A549	lung:	n/a	n/a
18	ATF3	chr9:12814089-12814909	HCT-116	colon:	n/a	n/a
19	ATF3	chr9:12814080-12814958	HCT-116	colon:	n/a	n/a
20	BACH1	chr9:12775963-12776675	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr9:12784589-12784652	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr9:12784537-12784775	K562	blood:	n/a	n/a
23	BATF	chr9:12784487-12784808	GM12878	blood:	n/a	chr9:12784627-12784638
24	BATF	chr9:12784440-12784836	GM12878	blood:	n/a	chr9:12784627-12784638
25	BCL11A	chr9:12784486-12784786	GM12878	blood:	n/a	n/a
26	BCL3	chr9:12813964-12815230	A549	lung:	n/a	chr9:12814953-12814962
27	BCL3	chr9:12814100-12814872	A549	lung:	n/a	n/a
28	BCL3	chr9:12774751-12775592	A549	lung:	n/a	chr9:12775208-12775217
29	BCL3	chr9:12775944-12776770	A549	lung:	n/a	chr9:12776114-12776127
30	BCL3	chr9:12784221-12785015	A549	lung:	n/a	n/a
31	BCL3	chr9:12794096-12794785	A549	lung:	n/a	n/a
32	BCL3	chr9:12784331-12785068	A549	lung:	n/a	n/a
33	BCL3	chr9:12775887-12777064	A549	lung:	n/a	chr9:12776114-12776127
34	BHLHE40	chr9:12771808-12772164	A549	lung:	n/a	n/a
35	BHLHE40	chr9:12814481-12814829	K562	blood:	n/a	n/a
36	BHLHE40	chr9:12776329-12776638	K562	blood:	n/a	n/a
37	BHLHE40	chr9:12776058-12776346	HepG2	liver:	n/a	n/a
38	BHLHE40	chr9:12827183-12827244	A549	lung:	n/a	n/a
39	BHLHE40	chr9:12784391-12784791	K562	blood:	n/a	n/a
40	BHLHE40	chr9:12814145-12814857	A549	lung:	n/a	n/a
41	BHLHE40	chr9:12784559-12784788	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:12784373-12785060	HepG2	liver:	n/a	n/a
43	BHLHE40	chr9:12816828-12817176	HepG2	liver:	n/a	n/a
44	BHLHE40	chr9:12816834-12817221	HepG2	liver:	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	chr9:12814024-12814857	HepG2	liver:	n/a	n/a
48	BRCA1	chr9:12776076-12776725	HepG2	liver:	n/a	n/a
49	BRCA1	chr9:12784182-12784865	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr9:12776070-12777883	Hela-S3	cervix:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:12774985-12775035	Caco-2	colon:	n/a
2	chr9:12776218-12776268	Caco-2	colon:	n/a
3	chr9:12774985-12775035	NH-A	brain:	n/a
4	chr9:12776218-12776268	BJ	skin:	n/a
5	chr9:12775700-12775750	HNPCEpiC	eye:	n/a
6	chr9:12775750-12775800	HEK293	kidney:	embryo
7	chr9:12774985-12775035	HRCEpiC	kidney:	n/a
8	chr9:12776218-12776268	HCF	heart:	n/a
9	chr9:12776046-12776096	K562	blood:	n/a
10	chr9:12774985-12775035	MCF10A-Er-Src	breast:	n/a
11	chr9:12776046-12776096	AG04449	skin:	fetal
12	chr9:12776218-12776268	Hepatocyte	liver:	n/a
13	chr9:12775750-12775800	GM12878	blood:	n/a
14	chr9:12774985-12775035	HL-60	blood:	n/a
15	chr9:12776046-12776096	HPAEpiC	pulmonary alveolar:	n/a
16	chr9:12774985-12775035	K562	blood:	n/a
17	chr9:12776046-12776096	NHBE	bronchial:	n/a
18	chr9:12775700-12775750	Jurkat	blood:	n/a
19	chr9:12776218-12776268	SK-N-SH	brain:	n/a
20	chr9:12775700-12775750	GM19239	blood:	n/a
21	chr9:12774985-12775035	Jurkat	blood:	n/a
22	chr9:12774985-12775035	AG09309	skin:	n/a
23	chr9:12776218-12776268	AG09309	skin:	n/a
24	chr9:12775700-12775750	NH-A	brain:	n/a
25	chr9:12775700-12775750	U87	brain:	n/a
26	chr9:12776046-12776096	LNCaP	prostate:	n/a
27	chr9:12775750-12775800	HIPEpiC	eye:	n/a
28	chr9:12775700-12775750	PANC-1	pancreas:	n/a
29	chr9:12775700-12775750	PrEC	prostate:	n/a
30	chr9:12774985-12775035	AoSMC	blood vessel:	n/a
31	chr9:12775700-12775750	HRE	kidney:	n/a
32	chr9:12776218-12776268	HUVEC	blood vessel:	n/a
33	chr9:12776218-12776268	BE2_C	brain:	n/a
34	chr9:12774985-12775035	PrEC	prostate:	n/a
35	chr9:12774985-12775035	HCM	heart:	n/a
36	chr9:12775700-12775750	NHBE	bronchial:	n/a
37	chr9:12776046-12776096	ovcar-3	ovarian:	n/a
38	chr9:12774985-12775035	SK-N-SH_RA	brain:	n/a
39	chr9:12776218-12776268	HNPCEpiC	eye:	n/a
40	chr9:12774985-12775035	CMK	blood:	n/a
41	chr9:12774985-12775035	HepG2	liver:	n/a
42	chr9:12775750-12775800	ECC-1	luminal epithelium:	n/a
43	chr9:12776218-12776268	SK-N-SH_RA	brain:	n/a
44	chr9:12775750-12775800	H1-hESC	embryonic stem cell:	embryo
45	chr9:12774985-12775035	NHDF-neo	bronchial:	n/a
46	chr9:12775750-12775800	BJ	skin:	n/a
47	chr9:12775750-12775800	HEEpiC	esophagus:	n/a
48	chr9:12775700-12775750	ECC-1	luminal epithelium:	n/a
49	chr9:12775700-12775750	HPAEpiC	pulmonary alveolar:	n/a
50	chr9:12775700-12775750	HMEC	breast:	n/a

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:12768044..12770724-chr9:12775061..12776621,2	MCF-7	breast:
2	chr9:12771458..12774120-chr9:12775878..12777874,2	K562	blood:
3	chr9:12774525..12776496-chr9:12779870..12781458,2	MCF-7	breast:
4	chr9:12816711..12819917-chr9:12821131..12823680,3	MCF-7	breast:
5	chr9:12784767..12786871-chr9:12796425..12798748,2	MCF-7	breast:
6	chr9:12794075..12796517-chr9:12813544..12816073,2	MCF-7	breast:
7	chr9:12777697..12781582-chr9:12805623..12809956,4	MCF-7	breast:
8	chr19:32895532..32897847-chr9:12774427..12776236,2	MCF-7	breast:
9	chr9:12817203..12820022-chr9:12879979..12881998,2	MCF-7	breast:
10	chr9:12719062..12719862-chr9:12884578..12885277,2	MCF-7	breast:
11	chr9:12809497..12811104-chr9:12812287..12814300,2	MCF-7	breast:
12	chr9:12796888..12798629-chr9:12811320..12813907,2	MCF-7	breast:
13	chr9:12794123..12798425-chr9:12799018..12802796,5	MCF-7	breast:
14	chr9:12773830..12776093-chr9:12831481..12833601,2	MCF-7	breast:
15	chr9:12779288..12781566-chr9:12835012..12836710,2	MCF-7	breast:
16	chr9:12719485..12720037-chr9:12987933..12988498,2	MCF-7	breast:
17	chr9:12770939..12774696-chr9:12774747..12779041,5	MCF-7	breast:
18	chr9:5854256..5856803-chr9:12790614..12793175,2	MCF-7	breast:
19	chr9:12793649..12798936-chr9:12813991..12818779,7	MCF-7	breast:
20	chr9:12748565..12752577-chr9:12774636..12778893,4	MCF-7	breast:
21	chr9:12794502..12796197-chr9:13084693..13086368,2	MCF-7	breast:
22	chr9:12715023..12717622-chr9:12718396..12720573,2	MCF-7	breast:
23	chr9:12816711..12819917-chr9:12821131..12823680,3	MCF-7	breast:
24	chr9:12788809..12790728-chr9:12792217..12794767,4	MCF-7	breast:
25	chr9:12723685..12724314-chr9:12988034..12988919,3	MCF-7	breast:
26	chr9:12816957..12819670-chr9:12821766..12823551,2	MCF-7	breast:
27	chr9:12732393..12734244-chr9:12774652..12776497,2	MCF-7	breast:
28	chr9:12723451..12724539-chr9:12884675..12885414,3	MCF-7	breast:
29	chr9:12785493..12787579-chr9:12811391..12813312,2	MCF-7	breast:
30	chr9:12786137..12788108-chr9:12801967..12804015,2	MCF-7	breast:
31	chr9:12774109..12791345-chr9:12812800..12822770,37	MCF-7	breast:
32	chr9:12778616..12780365-chr9:12854007..12856066,2	MCF-7	breast:
33	chr9:12729225..12731478-chr9:12790178..12792905,2	MCF-7	breast:
34	chr9:12750217..12752763-chr9:12757622..12759170,2	MCF-7	breast:
35	chr9:12816957..12819670-chr9:12821766..12823551,2	MCF-7	breast:
36	chr9:12773969..12780098-chr9:12789328..12796142,13	MCF-7	breast:
37	chr9:12784573..12785102-chr9:12794160..12794796,2	MCF-7	breast:
38	chr9:12788711..12790306-chr9:12792707..12794507,2	K562	blood:
39	chr9:12733476..12735004-chr9:12774992..12776567,2	MCF-7	breast:
40	chr9:12779288..12781566-chr9:12835012..12836710,2	MCF-7	breast:
41	chr9:12809497..12811104-chr9:12812287..12814300,2	MCF-7	breast:
42	chr9:12815854..12818984-chr9:12830927..12834079,3	MCF-7	breast:
43	chr9:12776291..12778540-chr9:12858744..12861808,3	MCF-7	breast:
44	chr9:12716514..12718700-chr9:12776478..12778096,2	MCF-7	breast:
45	chr9:12777697..12781582-chr9:12805623..12809956,4	MCF-7	breast:
46	chr9:12715023..12717622-chr9:12718396..12720573,2	MCF-7	breast:
47	chr9:12723856..12726602-chr9:12884690..12886916,2	MCF-7	breast:
48	chr9:12737180..12738894-chr9:12739213..12741322,2	MCF-7	breast:
49	chr16:50402392..50404309-chr9:12828030..12829558,2	MCF-7	breast:
50	chr9:12752690..12755433-chr9:12775370..12778156,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf150-1	chr9:12768922-12770158	XLOC_007283
2	lnc-C9orf150-1	chr9:12738519-12738662	XLOC_007283
3	lnc-MPDZ-8	chr9:12764762-12765054	NONHSAT130228
4	lnc-MPDZ-1	chr9:12790619-12790764	ENSG00000235448.1
5	lnc-C9orf150-2	chr9:12759301-12759537	l_3734_chr9:12728518-12759537_heart
6	lnc-C9orf150-2	chr9:12728519-12728662	l_3734_chr9:12728518-12759537_heart
7	lnc-MPDZ-1	chr9:12759551-12759623	ENSG00000235448.1
8	lnc-C9orf150-2	chr9:12758922-12759300	l_3734_chr9:12728518-12759537_heart
9	lnc-MPDZ-1	chr9:12814292-12814344	ENSG00000235448.1

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
ENSG00000223621	chromatin interactions
ENSG00000267213	chromatin interactions
ENSG00000261393	chromatin interactions
ENSG00000166164	chromatin interactions
ENSG00000235448	chromatin interactions
ENSG00000153714	chromatin interactions
ENSG00000269093	chromatin interactions
ENSG00000178904	chromatin interactions
ENSG00000222658	chromatin interactions

Extended variants
information (count: 5903 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:5903 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12379024	chr9:12717405-12717406	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs78230976	chr9:12717453-12717454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560657588	chr9:12717462-12717463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572750815	chr9:12717463-12717464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545180499	chr9:12717479-12717480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564891948	chr9:12717517-12717518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140138672	chr9:12717536-12717537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142972716	chr9:12717547-12717548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190047632	chr9:12717556-12717557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529283847	chr9:12717560-12717561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549545576	chr9:12717586-12717587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532174353	chr9:12717590-12717591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552438224	chr9:12717623-12717624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559874895	chr9:12717697-12717698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192138980	chr9:12717710-12717711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs117894711	chr9:12717761-12717762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150703804	chr9:12717770-12717771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537766273	chr9:12717785-12717786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184682022	chr9:12717852-12717853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114034012	chr9:12717871-12717872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548512509	chr9:12717882-12717883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs13295868	chr9:12717912-12717913	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs552691783	chr9:12717922-12717923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370189584	chr9:12717952-12717953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572613811	chr9:12717972-12717973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533802334	chr9:12718015-12718016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547139631	chr9:12718061-12718062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570559921	chr9:12718109-12718110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575328843	chr9:12718129-12718130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374383140	chr9:12718168-12718169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544521697	chr9:12718230-12718231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561162850	chr9:12718231-12718232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574123599	chr9:12718238-12718239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543049902	chr9:12718260-12718261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111918602	chr9:12718296-12718297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528605866	chr9:12718308-12718309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7019226	chr9:12718370-12718371	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs569261625	chr9:12718376-12718377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149780121	chr9:12718401-12718402	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs565510833	chr9:12718498-12718499	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs530991934	chr9:12718502-12718503	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs550912415	chr9:12718547-12718548	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs558774885	chr9:12718564-12718565	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs567613048	chr9:12718571-12718572	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs188613244	chr9:12718610-12718611	Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538111494	chr9:12718625-12718626	Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546192828	chr9:12718669-12718670	Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77308929	chr9:12718695-12718696	Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538759065	chr9:12718696-12718697	Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558347131	chr9:12718704-12718705	Flanking Active TSS Active TSS Enhancers Weak transcription	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Bipolar disorder	19114987	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:1932 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12709200-12718400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr9:12711200-12722400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:12716200-12718400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:12717000-12719000	Enhancers	HUVEC	blood vessel
5	chr9:12717400-12717800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr9:12717400-12718400	Weak transcription	Fetal Brain Female	brain
7	chr9:12717600-12717800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr9:12717800-12718200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr9:12717800-12718400	Enhancers	Fetal Brain Male	brain
10	chr9:12717800-12718600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr9:12717800-12718800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr9:12718000-12718200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:12718000-12718800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr9:12718200-12718400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr9:12718200-12718400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:12718200-12718400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr9:12718200-12718400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr9:12718200-12718400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr9:12718200-12718400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr9:12718200-12718400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr9:12718200-12718400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:12718200-12718400	Enhancers	HSMMtube	muscle
23	chr9:12718200-12718400	Enhancers	NH-A	brain
24	chr9:12718200-12719200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr9:12718200-12719600	Enhancers	Fetal Heart	heart
26	chr9:12718400-12718600	Enhancers	H1 Cell Line	embryonic stem cell
27	chr9:12718400-12718600	Enhancers	H9 Cell Line	embryonic stem cell
28	chr9:12718400-12718600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr9:12718400-12718600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr9:12718400-12718600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr9:12718400-12718600	Enhancers	Brain Germinal Matrix	brain
32	chr9:12718400-12718600	Enhancers	Brain Substantia Nigra	brain
33	chr9:12718400-12718600	Enhancers	Fetal Brain Female	brain
34	chr9:12718400-12718600	Enhancers	Osteobl	bone
35	chr9:12718400-12718800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr9:12718400-12718800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr9:12718400-12718800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr9:12718400-12718800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr9:12718400-12718800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr9:12718400-12718800	Enhancers	Primary hematopoietic stem cells	blood
41	chr9:12718400-12718800	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr9:12718400-12718800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr9:12718400-12718800	Flanking Active TSS	Fetal Brain Male	brain
44	chr9:12718400-12718800	Enhancers	Lung	lung
45	chr9:12718400-12718800	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr9:12718400-12718800	Enhancers	Spleen	Spleen
47	chr9:12718400-12718800	Flanking Active TSS	HSMMtube	muscle
48	chr9:12718400-12719000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:12718400-12719000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:12718400-12719000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell

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