Variant report

Variant	nsv1041424
Chromosome Location	chr9:115389428-115590950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3464)
CpG islands
(count:854)
Chromatin interactive
region (count:226)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3464 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115512832-115512868	K562	blood:	n/a	n/a
2	ARID3A	chr9:115527085-115527557	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:115480786-115481091	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:115480303-115480518	K562	blood:	n/a	n/a
5	ARID3A	chr9:115509251-115509790	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:115480237-115480501	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:115494056-115494755	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:115526787-115526979	K562	blood:	n/a	n/a
9	ARID3A	chr9:115512431-115512988	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:115479963-115479990	K562	blood:	n/a	n/a
11	ATF1	chr9:115479899-115480664	K562	blood:	n/a	n/a
12	ATF1	chr9:115546849-115547018	K562	blood:	n/a	n/a
13	ATF1	chr9:115492920-115493063	K562	blood:	n/a	n/a
14	ATF2	chr9:115480059-115480571	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr9:115536387-115537342	GM12878	blood:	n/a	n/a
16	ATF2	chr9:115479969-115480608	GM12878	blood:	n/a	n/a
17	ATF2	chr9:115571553-115572322	GM12878	blood:	n/a	n/a
18	ATF2	chr9:115533877-115534620	GM12878	blood:	n/a	n/a
19	ATF2	chr9:115546557-115547024	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr9:115571491-115572271	GM12878	blood:	n/a	n/a
21	ATF2	chr9:115534041-115534389	GM12878	blood:	n/a	n/a
22	ATF2	chr9:115461473-115461858	GM12878	blood:	n/a	n/a
23	ATF2	chr9:115546485-115546980	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr9:115461429-115461926	GM12878	blood:	n/a	n/a
25	ATF2	chr9:115479964-115480574	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr9:115512764-115513021	K562	blood:	n/a	n/a
27	ATF3	chr9:115513811-115514038	K562	blood:	n/a	chr9:115513959-115513968
28	BACH1	chr9:115555648-115555803	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr9:115480689-115480847	K562	blood:	n/a	n/a
30	BACH1	chr9:115391691-115391696	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr9:115480800-115481000	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr9:115513425-115513999	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr9:115477422-115477655	GM12878	blood:	n/a	n/a
34	BATF	chr9:115450305-115450695	GM12878	blood:	n/a	chr9:115450534-115450545 chr9:115450535-115450545
35	BATF	chr9:115555592-115555842	GM12878	blood:	n/a	n/a
36	BATF	chr9:115571596-115572164	GM12878	blood:	n/a	chr9:115571860-115571871
37	BATF	chr9:115571549-115572196	GM12878	blood:	n/a	chr9:115571860-115571871
38	BATF	chr9:115481594-115481937	GM12878	blood:	n/a	n/a
39	BATF	chr9:115481521-115481962	GM12878	blood:	n/a	n/a
40	BATF	chr9:115477441-115477621	GM12878	blood:	n/a	n/a
41	BCL11A	chr9:115571502-115572209	GM12878	blood:	n/a	n/a
42	BCL11A	chr9:115571550-115572162	GM12878	blood:	n/a	n/a
43	BCL3	chr9:115461526-115461832	GM12878	blood:	n/a	n/a
44	BCL3	chr9:115571588-115572096	GM12878	blood:	n/a	n/a
45	BCLAF1	chr9:115479865-115480402	GM12878	blood:	n/a	n/a
46	BCLAF1	chr9:115461422-115462143	GM12878	blood:	n/a	n/a
47	BCLAF1	chr9:115479702-115480535	GM12878	blood:	n/a	chr9:115480429-115480442
48	BCLAF1	chr9:115512540-115513253	GM12878	blood:	n/a	chr9:115513227-115513236 chr9:115513036-115513049 chr9:115513132-115513145
49	BCLAF1	chr9:115582032-115582507	GM12878	blood:	n/a	n/a
50	BCLAF1	chr9:115571497-115572306	GM12878	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115512530-115512580	HCPEpiC	choroid plexus:	n/a
2	chr9:115480060-115480110	HEK293	kidney:	embryo
3	chr9:115512612-115512662	MCF-7	breast:	n/a
4	chr9:115513820-115513870	HCM	heart:	n/a
5	chr9:115513056-115513106	K562	blood:	n/a
6	chr9:115480625-115480675	ProgFib	skin:	n/a
7	chr9:115480060-115480110	HCT-116	colon:	n/a
8	chr9:115480539-115480589	ProgFib	skin:	n/a
9	chr9:115509770-115509820	HepG2	liver:	n/a
10	chr9:115480625-115480675	HCT-116	colon:	n/a
11	chr9:115480539-115480589	HNPCEpiC	eye:	n/a
12	chr9:115513482-115513532	HepG2	liver:	n/a
13	chr9:115481039-115481089	HIPEpiC	eye:	n/a
14	chr9:115480630-115480680	Hela-S3	cervix:	n/a
15	chr9:115513525-115513575	AG10803	skin:	n/a
16	chr9:115512612-115512662	HCPEpiC	choroid plexus:	n/a
17	chr9:115480324-115480374	NB4	blood:	n/a
18	chr9:115509770-115509820	ProgFib	skin:	n/a
19	chr9:115513756-115513806	HL-60	blood:	n/a
20	chr9:115513756-115513806	HRCEpiC	kidney:	n/a
21	chr9:115480060-115480110	ECC-1	luminal epithelium:	n/a
22	chr9:115480060-115480110	ProgFib	skin:	n/a
23	chr9:115512612-115512662	GM06990	blood:	n/a
24	chr9:115480625-115480675	HCM	heart:	n/a
25	chr9:115513056-115513106	AoSMC	blood vessel:	n/a
26	chr9:115513482-115513532	T-47D	breast:	n/a
27	chr9:115513756-115513806	PrEC	prostate:	n/a
28	chr9:115512612-115512662	NHBE	bronchial:	n/a
29	chr9:115513482-115513532	IMR90	lung:	fetal
30	chr9:115513056-115513106	HRCEpiC	kidney:	n/a
31	chr9:115480625-115480675	IMR90	lung:	fetal
32	chr9:115512612-115512662	HNPCEpiC	eye:	n/a
33	chr9:115513525-115513575	AG09319	gingival:	n/a
34	chr9:115509770-115509820	Hepatocyte	liver:	n/a
35	chr9:115513820-115513870	NHDF-neo	bronchial:	n/a
36	chr9:115480539-115480589	HepG2	liver:	n/a
37	chr9:115513820-115513870	GM19239	blood:	n/a
38	chr9:115480324-115480374	ProgFib	skin:	n/a
39	chr9:115509770-115509820	GM12892	blood:	n/a
40	chr9:115513525-115513575	NHBE	bronchial:	n/a
41	chr9:115513482-115513532	RPTEC	kidney:	n/a
42	chr9:115480324-115480374	NHBE	bronchial:	n/a
43	chr9:115513482-115513532	HEK293	kidney:	embryo
44	chr9:115481039-115481089	Hela-S3	cervix:	n/a
45	chr9:115509770-115509820	GM19239	blood:	n/a
46	chr9:115513525-115513575	HMEC	breast:	n/a
47	chr9:115513820-115513870	AG09309	skin:	n/a
48	chr9:115480625-115480675	NT2-D1	testis:	n/a
49	chr9:115480060-115480110	HRE	kidney:	n/a
50	chr9:115480060-115480110	GM12891	blood:	n/a

(count:226 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr9:115363911..115365862-chr9:115389104..115390742,2	K562	blood:
2	chr9:115498256..115499821-chr9:115502701..115504658,2	MCF-7	breast:
3	chr9:115565373..115568100-chr9:115582412..115584863,2	MCF-7	breast:
4	chr9:115568430..115571071-chr9:115577497..115580948,3	MCF-7	breast:
5	chr9:115555372..115556213-chr9:115581844..115582573,3	MCF-7	breast:
6	chr9:115496362..115499450-chr9:115509483..115512826,3	K562	blood:
7	chr9:115543121..115545474-chr9:115548889..115551043,2	K562	blood:
8	chr9:115472706..115474595-chr9:115477328..115479365,2	K562	blood:
9	chr9:115425089..115427194-chr9:115429213..115432033,2	K562	blood:
10	chr9:115401662..115403762-chr9:115408579..115410766,2	K562	blood:
11	chr9:115552552..115554676-chr9:115556505..115559633,3	MCF-7	breast:
12	chr9:114849146..114849653-chr9:115555183..115555717,2	K562	blood:
13	chr9:115505654..115506184-chr9:115665140..115665712,2	MCF-7	breast:
14	chr9:115534861..115537925-chr9:115540163..115544235,3	MCF-7	breast:
15	chr9:115543121..115545474-chr9:115548889..115551043,2	K562	blood:
16	chr9:115505232..115509202-chr9:115509878..115514316,6	K562	blood:
17	chr9:115533906..115536575-chr9:115567141..115568722,2	MCF-7	breast:
18	chr9:115542323..115543892-chr9:115545474..115547035,2	K562	blood:
19	chr9:115491320..115493108-chr9:115519478..115521653,2	MCF-7	breast:
20	chr1:9294148..9295084-chr9:115512424..115513185,2	Hela-S3	cervix:
21	chr9:115549006..115551974-chr9:115557854..115560441,2	K562	blood:
22	chr9:115571216..115573226-chr9:115575838..115578800,2	K562	blood:
23	chr9:115205537..115206125-chr9:115473120..115473635,2	MCF-7	breast:
24	chr9:115463918..115467105-chr9:115470637..115474158,3	K562	blood:
25	chr9:115496362..115497969-chr9:115509483..115511853,2	K562	blood:
26	chr9:115457842..115461023-chr9:115478755..115482028,3	K562	blood:
27	chr9:115513405..115514933-chr9:115545989..115548662,2	MCF-7	breast:
28	chr9:115479584..115483073-chr9:115511753..115516407,5	MCF-7	breast:
29	chr9:115534861..115537925-chr9:115540163..115544235,3	MCF-7	breast:
30	chr9:115449599..115451431-chr9:115473540..115475115,2	K562	blood:
31	chr9:115581292..115584107-chr9:115597875..115599534,2	MCF-7	breast:
32	chr9:114849487..114850237-chr9:115427590..115428335,2	MCF-7	breast:
33	chr20:55839378..55840930-chr9:115479448..115481432,2	MCF-7	breast:
34	chr9:115247539..115250274-chr9:115478530..115480518,2	K562	blood:
35	chr9:115205263..115206168-chr9:115581964..115582608,2	MCF-7	breast:
36	chr9:115571216..115573226-chr9:115575838..115578800,2	K562	blood:
37	chr9:115456646..115458575-chr9:115460716..115463371,2	MCF-7	breast:
38	chr9:115446137..115448834-chr9:115451791..115453700,3	K562	blood:
39	chr9:115249020..115249928-chr9:115479752..115480523,2	Hela-S3	cervix:
40	chr9:115361438..115362990-chr9:115407331..115409341,2	MCF-7	breast:
41	chr9:115529521..115533265-chr9:115533546..115536712,4	K562	blood:
42	chr9:115421830..115423698-chr9:115425235..115427164,2	K562	blood:
43	chr9:115466699..115468556-chr9:115477154..115479875,2	K562	blood:
44	chr9:115511729..115513827-chr9:115524619..115527032,2	K562	blood:
45	chr9:115552552..115554676-chr9:115556505..115559633,3	MCF-7	breast:
46	chr9:115473082..115474008-chr9:115511306..115512239,2	K562	blood:
47	chr9:115398005..115400078-chr9:115404620..115406595,2	MCF-7	breast:
48	chr9:115235092..115237289-chr9:115391747..115394330,2	K562	blood:
49	chr9:115512316..115514216-chr9:115529153..115530836,3	MCF-7	breast:
50	chr9:115529521..115533265-chr9:115533546..115536712,4	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA1958-1	chr9:115484007-115484956	NONHSAT134022
2	lnc-SLC46A2-4	chr9:115480267-115480397	NONHSAT134023
3	lnc-KIAA1958-1	chr9:115454118-115454181	NONHSAT134022
4	lnc-SNX30-2	chr9:115390750-115391983	NONHSAT134020
5	lnc-C9orf80-1	chr9:115505051-115505514	XLOC_007830
6	lnc-KIAA1958-1	chr9:115453057-115453265	NONHSAT134022
7	lnc-C9orf80-1	chr9:115512686-115512736	XLOC_007830
8	lnc-C9orf80-1	chr9:115511182-115511550	XLOC_007830
9	lnc-SLC46A2-4	chr9:115478741-115478821	NONHSAT134023
10	lnc-SLC46A2-4	chr9:115456314-115456513	NONHSAT134023
11	lnc-C9orf80-1	chr9:115511360-115512795	XLOC_007830

No data

Variant related genes	Relation type
ENSG00000226609	TF binding region
INIP	TF binding region
SNX30	TF binding region
ENSG00000226609	CpG island
INIP	CpG island
SNX30	CpG island
ENSG00000148158	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000049239	chromatin interactions
ENSG00000165185	chromatin interactions
ENSG00000110925	chromatin interactions
ENSG00000230185	chromatin interactions
ENSG00000010165	chromatin interactions
ENSG00000119471	chromatin interactions
ENSG00000271631	chromatin interactions
ENSG00000226609	chromatin interactions
ENSG00000119314	chromatin interactions
ENSG00000148153	chromatin interactions
ENSG00000173473	chromatin interactions
ENSG00000150760	chromatin interactions
SETD8	miRNA target sites

Extended variants
information (count: 7439 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:7439 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530943296	chr9:115389437-115389438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375522122	chr9:115389475-115389476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191689148	chr9:115389492-115389493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530256107	chr9:115389515-115389516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549180974	chr9:115389523-115389524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184201100	chr9:115389526-115389527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188824482	chr9:115389546-115389547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201365677	chr9:115389609-115389610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368587890	chr9:115389678-115389679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551665987	chr9:115389684-115389685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34853292	chr9:115389741-115389742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs180863364	chr9:115389750-115389751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11792981	chr9:115389767-115389768	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs556722767	chr9:115389848-115389849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573386627	chr9:115389886-115389887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs62575201	chr9:115389914-115389915	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186189538	chr9:115389943-115389944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573117001	chr9:115389953-115389954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186473471	chr9:115389964-115389965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34557800	chr9:115389965-115389966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545336051	chr9:115389978-115389979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190318496	chr9:115389995-115389996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4979139	chr9:115390037-115390038	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs575891979	chr9:115390142-115390143	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544582947	chr9:115390169-115390170	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182448916	chr9:115390190-115390191	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146870909	chr9:115390215-115390216	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs547134051	chr9:115390247-115390248	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs186634937	chr9:115390264-115390265	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs528300860	chr9:115390315-115390316	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs551333422	chr9:115390356-115390357	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs571509110	chr9:115390359-115390360	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs190516042	chr9:115390393-115390394	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs16917155	chr9:115390448-115390449	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs10981459	chr9:115390449-115390450	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs535908943	chr9:115390477-115390478	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs552659351	chr9:115390481-115390482	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs573054151	chr9:115390482-115390483	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs527256825	chr9:115390488-115390489	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs532894820	chr9:115390489-115390490	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs558923598	chr9:115390505-115390506	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs552256096	chr9:115390580-115390581	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs182393919	chr9:115390604-115390605	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs117582031	chr9:115390618-115390619	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs138941209	chr9:115390685-115390686	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs574897818	chr9:115390690-115390691	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs148939190	chr9:115390726-115390727	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs143647177	chr9:115390742-115390743	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs532538787	chr9:115390813-115390814	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs550881366	chr9:115390815-115390816	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4788 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115368600-115391600	Weak transcription	Brain Hippocampus Middle	brain
2	chr9:115379000-115391400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr9:115379000-115410200	Weak transcription	HSMMtube	muscle
4	chr9:115380000-115392000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr9:115381000-115392600	Weak transcription	Left Ventricle	heart
6	chr9:115381000-115402800	Weak transcription	Primary T cells from cord blood	blood
7	chr9:115381200-115391800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:115381200-115392000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr9:115381200-115392200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr9:115381200-115392200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:115381200-115392200	Weak transcription	Fetal Stomach	stomach
12	chr9:115381200-115393400	Weak transcription	Primary B cells from cord blood	blood
13	chr9:115381200-115393400	Weak transcription	Fetal Muscle Trunk	muscle
14	chr9:115381200-115393400	Weak transcription	Fetal Muscle Leg	muscle
15	chr9:115381200-115400600	Weak transcription	Fetal Intestine Small	intestine
16	chr9:115381200-115401600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr9:115381200-115401600	Weak transcription	Dnd41	blood
18	chr9:115383000-115399800	Weak transcription	Gastric	stomach
19	chr9:115383600-115392200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr9:115383600-115392200	Weak transcription	K562	blood
21	chr9:115383600-115401400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr9:115386200-115390000	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr9:115387200-115390200	Weak transcription	Brain Substantia Nigra	brain
24	chr9:115387200-115391600	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr9:115387200-115391600	Weak transcription	Brain Germinal Matrix	brain
26	chr9:115387200-115391800	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr9:115387200-115392000	Weak transcription	Brain Cingulate Gyrus	brain
28	chr9:115387400-115392000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr9:115387400-115392000	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr9:115387600-115392200	Weak transcription	Brain Anterior Caudate	brain
31	chr9:115387600-115401400	Weak transcription	Esophagus	oesophagus
32	chr9:115387800-115392000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr9:115388000-115401400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:115389200-115389800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:115389200-115390600	Enhancers	Ovary	ovary
36	chr9:115389800-115391200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr9:115390000-115391000	Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr9:115390200-115390600	Enhancers	Brain Substantia Nigra	brain
39	chr9:115390400-115390600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr9:115390400-115392200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:115390600-115392000	Weak transcription	Brain Substantia Nigra	brain
42	chr9:115390600-115392200	Weak transcription	Ovary	ovary
43	chr9:115390800-115392000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr9:115391000-115392000	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr9:115391200-115392400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr9:115391400-115392600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr9:115391600-115392600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr9:115391600-115392600	Enhancers	Adipose Nuclei	Adipose
49	chr9:115391600-115392600	Enhancers	Brain Germinal Matrix	brain
50	chr9:115391600-115392600	Enhancers	Brain Hippocampus Middle	brain

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