Variant report

Variant	nsv915763
Chromosome Location	chr9:115379600-115588349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3503)
CpG islands
(count:856)
Chromatin interactive
region (count:232)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3503 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115480303-115480518	K562	blood:	n/a	n/a
2	ARID3A	chr9:115480237-115480501	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:115527085-115527557	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:115512832-115512868	K562	blood:	n/a	n/a
5	ARID3A	chr9:115526787-115526979	K562	blood:	n/a	n/a
6	ARID3A	chr9:115509251-115509790	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:115479963-115479990	K562	blood:	n/a	n/a
8	ARID3A	chr9:115480786-115481091	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:115512431-115512988	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:115494056-115494755	HepG2	liver:	n/a	n/a
11	ATF1	chr9:115546849-115547018	K562	blood:	n/a	n/a
12	ATF1	chr9:115479899-115480664	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	chr9:115571553-115572322	GM12878	blood:	n/a	n/a
17	ATF2	chr9:115571491-115572271	GM12878	blood:	n/a	n/a
18	ATF2	chr9:115479969-115480608	GM12878	blood:	n/a	n/a
19	ATF2	chr9:115461473-115461858	GM12878	blood:	n/a	n/a
20	ATF2	chr9:115479964-115480574	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr9:115546485-115546980	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr9:115461429-115461926	GM12878	blood:	n/a	n/a
23	ATF2	chr9:115533877-115534620	GM12878	blood:	n/a	n/a
24	ATF2	chr9:115534041-115534389	GM12878	blood:	n/a	n/a
25	ATF2	chr9:115546557-115547024	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	chr9:115391691-115391696	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr9:115513425-115513999	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr9:115480689-115480847	K562	blood:	n/a	n/a
31	BACH1	chr9:115383915-115383962	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr9:115480800-115481000	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr9:115555648-115555803	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr9:115450305-115450695	GM12878	blood:	n/a	chr9:115450534-115450545 chr9:115450535-115450545
35	BATF	chr9:115477422-115477655	GM12878	blood:	n/a	n/a
36	BATF	chr9:115481521-115481962	GM12878	blood:	n/a	n/a
37	BATF	chr9:115481594-115481937	GM12878	blood:	n/a	n/a
38	BATF	chr9:115571549-115572196	GM12878	blood:	n/a	chr9:115571860-115571871
39	BATF	chr9:115477441-115477621	GM12878	blood:	n/a	n/a
40	BATF	chr9:115555592-115555842	GM12878	blood:	n/a	n/a
41	BATF	chr9:115571596-115572164	GM12878	blood:	n/a	chr9:115571860-115571871
42	BCL11A	chr9:115571502-115572209	GM12878	blood:	n/a	n/a
43	BCL11A	chr9:115571550-115572162	GM12878	blood:	n/a	n/a
44	BCL3	chr9:115461526-115461832	GM12878	blood:	n/a	n/a
45	BCL3	chr9:115571588-115572096	GM12878	blood:	n/a	n/a
46	BCLAF1	chr9:115479702-115480535	GM12878	blood:	n/a	chr9:115480429-115480442
47	BCLAF1	chr9:115582032-115582507	GM12878	blood:	n/a	n/a
48	BCLAF1	chr9:115536629-115537207	GM12878	blood:	n/a	n/a
49	BCLAF1	chr9:115555367-115555922	GM12878	blood:	n/a	n/a
50	BCLAF1	chr9:115479865-115480402	GM12878	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115513756-115513806	HCF	heart:	n/a
2	chr9:115513820-115513870	SKMC	muscle:	n/a
3	chr9:115513756-115513806	HCF	heart:	n/a
4	chr9:115513820-115513870	SKMC	muscle:	n/a
5	chr9:115480060-115480110	SK-N-SH	brain:	n/a
6	chr9:115480625-115480675	HRCEpiC	kidney:	n/a
7	chr9:115512612-115512662	AG04450	lung:	fetal
8	chr9:115481039-115481089	HIPEpiC	eye:	n/a
9	chr9:115480630-115480680	A549	lung:	n/a
10	chr9:115509770-115509820	HL-60	blood:	n/a
11	chr9:115513525-115513575	GM12891	blood:	n/a
12	chr9:115480324-115480374	AG09319	gingival:	n/a
13	chr9:115480539-115480589	RPTEC	kidney:	n/a
14	chr9:115513756-115513806	H1-hESC	embryonic stem cell:	embryo
15	chr9:115513820-115513870	PrEC	prostate:	n/a
16	chr9:115480625-115480675	GM12878	blood:	n/a
17	chr9:115480630-115480680	T-47D	breast:	n/a
18	chr9:115481039-115481089	HCF	heart:	n/a
19	chr9:115512612-115512662	HPAEpiC	pulmonary alveolar:	n/a
20	chr9:115480060-115480110	Caco-2	colon:	n/a
21	chr9:115480324-115480374	HNPCEpiC	eye:	n/a
22	chr9:115481039-115481089	HL-60	blood:	n/a
23	chr9:115480324-115480374	HUVEC	blood vessel:	n/a
24	chr9:115480539-115480589	GM19239	blood:	n/a
25	chr9:115513056-115513106	HCM	heart:	n/a
26	chr9:115512612-115512662	MCF-7	breast:	n/a
27	chr9:115513756-115513806	PFSK-1	brain:	n/a
28	chr9:115513056-115513106	IMR90	lung:	fetal
29	chr9:115509770-115509820	GM06990	blood:	n/a
30	chr9:115480060-115480110	LNCaP	prostate:	n/a
31	chr9:115513482-115513532	SK-N-MC	brain:	n/a
32	chr9:115480630-115480680	H1-hESC	embryonic stem cell:	embryo
33	chr9:115513482-115513532	AoSMC	blood vessel:	n/a
34	chr9:115513525-115513575	PFSK-1	brain:	n/a
35	chr9:115513756-115513806	SK-N-SH_RA	brain:	n/a
36	chr9:115513482-115513532	HNPCEpiC	eye:	n/a
37	chr9:115513820-115513870	MCF-7	breast:	n/a
38	chr9:115481039-115481089	Caco-2	colon:	n/a
39	chr9:115512612-115512662	BJ	skin:	n/a
40	chr9:115480324-115480374	AG09309	skin:	n/a
41	chr9:115480324-115480374	HepG2	liver:	n/a
42	chr9:115512612-115512662	HRE	kidney:	n/a
43	chr9:115512530-115512580	LNCaP	prostate:	n/a
44	chr9:115480539-115480589	T-47D	breast:	n/a
45	chr9:115481039-115481089	HEK293	kidney:	embryo
46	chr9:115513820-115513870	HMEC	breast:	n/a
47	chr9:115480625-115480675	HRPEpiC	eye:	n/a
48	chr9:115513525-115513575	NT2-D1	testis:	n/a
49	chr9:115480060-115480110	HCM	heart:	n/a
50	chr9:115513056-115513106	HCPEpiC	choroid plexus:	n/a

(count:232 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr9:115401662..115403762-chr9:115408579..115410766,2	K562	blood:
2	chr9:115384018..115386931-chr9:115389351..115391854,2	K562	blood:
3	chr9:115542323..115543892-chr9:115545474..115547035,2	K562	blood:
4	chr9:115566993..115569306-chr9:115570718..115573402,2	K562	blood:
5	chr9:115204852..115206161-chr9:115427327..115428280,9	MCF-7	breast:
6	chr9:115205105..115205795-chr9:115467855..115468653,2	MCF-7	breast:
7	chr9:115447768..115450470-chr9:115455814..115458350,2	MCF-7	breast:
8	chr9:115449599..115451431-chr9:115473540..115475115,2	K562	blood:
9	chr9:115471879..115473939-chr9:115578770..115581300,2	MCF-7	breast:
10	chr9:115512086..115514376-chr9:115549215..115552051,3	MCF-7	breast:
11	chr9:115465332..115466995-chr9:115480196..115481737,2	K562	blood:
12	chr9:115383838..115387286-chr9:115392608..115396534,4	K562	blood:
13	chr20:55839378..55840930-chr9:115479448..115481432,2	MCF-7	breast:
14	chr9:115555506..115558401-chr9:115567192..115568729,2	MCF-7	breast:
15	chr9:115555096..115556091-chr9:115581952..115582779,4	MCF-7	breast:
16	chr9:115398005..115400078-chr9:115404620..115406595,2	MCF-7	breast:
17	chr9:115505189..115506150-chr9:115555231..115556122,11	MCF-7	breast:
18	chr9:115447768..115450470-chr9:115455814..115458350,2	MCF-7	breast:
19	chr9:115505654..115506184-chr9:115665140..115665712,2	MCF-7	breast:
20	chr9:115247434..115250274-chr9:115478530..115481434,2	K562	blood:
21	chr9:115505189..115506150-chr9:115555231..115556122,11	MCF-7	breast:
22	chr9:115505232..115509202-chr9:115509878..115514316,6	K562	blood:
23	chr9:115205537..115206125-chr9:115473120..115473635,2	MCF-7	breast:
24	chr9:115248674..115250547-chr9:115381858..115383773,2	K562	blood:
25	chr9:115512640..115515348-chr9:115547273..115548788,2	MCF-7	breast:
26	chr9:115449599..115451431-chr9:115473540..115475115,2	K562	blood:
27	chr9:115545454..115548524-chr9:115549503..115552233,3	MCF-7	breast:
28	chr9:115552552..115554676-chr9:115556505..115559633,3	MCF-7	breast:
29	chr9:115533346..115535894-chr9:115545369..115547662,2	MCF-7	breast:
30	chr9:115512422..115514539-chr9:115533926..115536411,4	MCF-7	breast:
31	chr9:115379161..115382087-chr9:115394727..115397180,2	K562	blood:
32	chr9:115529521..115533265-chr9:115533546..115536712,4	K562	blood:
33	chr9:115504115..115508206-chr9:115509964..115513846,5	MCF-7	breast:
34	chr9:115425089..115427194-chr9:115429213..115432033,2	K562	blood:
35	chr9:115578144..115579912-chr9:115585850..115587895,2	K562	blood:
36	chr9:115398901..115401113-chr9:115401178..115403996,2	K562	blood:
37	chr9:115568430..115571071-chr9:115577497..115580948,3	MCF-7	breast:
38	chr9:115505322..115506123-chr9:115581889..115582739,2	MCF-7	breast:
39	chr9:115446137..115448834-chr9:115451791..115453700,3	K562	blood:
40	chr9:115247555..115250048-chr9:115510709..115513501,2	K562	blood:
41	chr9:115452851..115454387-chr9:115511339..115512880,2	K562	blood:
42	chr9:115456646..115458575-chr9:115460716..115463371,2	MCF-7	breast:
43	chr9:115543121..115545474-chr9:115548889..115551043,2	K562	blood:
44	chr9:115549478..115551812-chr9:115554338..115556959,2	MCF-7	breast:
45	chr9:115570774..115572548-chr9:115577000..115579037,2	MCF-7	breast:
46	chr9:115465512..115468135-chr9:115469344..115471975,2	MCF-7	breast:
47	chr9:115463918..115467105-chr9:115470637..115474158,3	K562	blood:
48	chr9:115398005..115400078-chr9:115404620..115406595,2	MCF-7	breast:
49	chr9:115555053..115556635-chr9:115557312..115560299,2	MCF-7	breast:
50	chr9:115485448..115488278-chr9:115512375..115514169,2	MCF-7	breast:

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

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

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
ENSG00000165185	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000119471	chromatin interactions
ENSG00000049239	chromatin interactions
ENSG00000230185	chromatin interactions
ENSG00000226609	chromatin interactions
ENSG00000271631	chromatin interactions
ENSG00000150760	chromatin interactions
ENSG00000148158	chromatin interactions
ENSG00000119314	chromatin interactions
ENSG00000148153	chromatin interactions
ENSG00000010165	chromatin interactions
ENSG00000110925	chromatin interactions
ENSG00000173473	chromatin interactions
SETD8	miRNA target sites

Extended variants
information (count: 7659 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:7659 , 50 per page) page: 1 2 3 4 5 6 7 ... 154

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568888015	chr9:115379608-115379609	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533116361	chr9:115379752-115379753	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553588729	chr9:115379851-115379852	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs550309769	chr9:115379878-115379879	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs570021998	chr9:115379910-115379911	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs139823012	chr9:115379918-115379919	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs145349767	chr9:115379925-115379926	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs147283870	chr9:115379927-115379928	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs80266343	chr9:115379937-115379938	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs544909059	chr9:115380028-115380029	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs192852610	chr9:115380031-115380032	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs184770553	chr9:115380041-115380042	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs375175569	chr9:115380182-115380183	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs117026196	chr9:115380192-115380193	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs61747198	chr9:115380212-115380213	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576034981	chr9:115380245-115380246	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541845355	chr9:115380296-115380297	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573906437	chr9:115380419-115380420	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368246788	chr9:115380454-115380455	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140803393	chr9:115380521-115380522	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563132307	chr9:115380596-115380597	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs199574594	chr9:115380691-115380692	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187708115	chr9:115380709-115380710	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192271994	chr9:115380722-115380723	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533181215	chr9:115380767-115380768	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200708381	chr9:115380770-115380771	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142182888	chr9:115380785-115380786	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs151187497	chr9:115380786-115380787	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183790667	chr9:115380800-115380801	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs76244866	chr9:115380809-115380810	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs565942160	chr9:115380820-115380821	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs189234731	chr9:115380899-115380900	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs77611284	chr9:115381144-115381145	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs3780687	chr9:115381164-115381165	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149946235	chr9:115381191-115381192	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562542332	chr9:115381206-115381207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373267558	chr9:115381266-115381267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537118908	chr9:115381302-115381303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557190137	chr9:115381330-115381331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576145631	chr9:115381375-115381376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181989895	chr9:115381413-115381414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184216389	chr9:115381468-115381469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572358810	chr9:115381549-115381550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541369142	chr9:115381551-115381552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146423730	chr9:115381557-115381558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140847943	chr9:115381560-115381561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs117295800	chr9:115381569-115381570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563241266	chr9:115381582-115381583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529032809	chr9:115381599-115381600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144599034	chr9:115381611-115381612	Weak transcription Strong transcription	n/a	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:4996 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115337600-115380200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:115338400-115379800	Weak transcription	Primary B cells from cord blood	blood
3	chr9:115344400-115380200	Weak transcription	Gastric	stomach
4	chr9:115346400-115385000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr9:115358200-115380000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr9:115359800-115380400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr9:115361400-115380200	Weak transcription	Fetal Intestine Small	intestine
8	chr9:115364000-115379800	Weak transcription	Ovary	ovary
9	chr9:115364000-115380200	Weak transcription	Aorta	Aorta
10	chr9:115365200-115380200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:115366000-115380200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr9:115368600-115391600	Weak transcription	Brain Hippocampus Middle	brain
13	chr9:115369200-115380200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr9:115370400-115380000	Weak transcription	Fetal Intestine Large	intestine
15	chr9:115370400-115380200	Weak transcription	Fetal Muscle Trunk	muscle
16	chr9:115373800-115380200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr9:115374600-115382200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:115375000-115380200	Weak transcription	Thymus	Thymus
19	chr9:115375200-115380200	Weak transcription	Pancreas	Pancrea
20	chr9:115375600-115380200	Weak transcription	Fetal Muscle Leg	muscle
21	chr9:115375600-115380600	Weak transcription	Left Ventricle	heart
22	chr9:115375600-115380800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr9:115376200-115379800	Weak transcription	Fetal Lung	lung
24	chr9:115376600-115380000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:115377200-115381400	Weak transcription	Right Atrium	heart
26	chr9:115377800-115380200	Weak transcription	K562	blood
27	chr9:115378000-115379800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr9:115378000-115380000	Weak transcription	Primary T cells from cord blood	blood
29	chr9:115378000-115383400	Weak transcription	GM12878-XiMat	blood
30	chr9:115378200-115379600	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr9:115378200-115380000	Weak transcription	Liver	Liver
32	chr9:115378200-115380000	Weak transcription	Fetal Thymus	thymus
33	chr9:115378200-115380200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr9:115378200-115380200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr9:115378400-115380000	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr9:115378400-115380000	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr9:115378400-115380200	Weak transcription	Fetal Stomach	stomach
38	chr9:115378400-115380200	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr9:115378400-115380200	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr9:115378400-115380400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr9:115378400-115382400	Weak transcription	A549	lung
42	chr9:115378400-115386600	Weak transcription	Brain Cingulate Gyrus	brain
43	chr9:115378600-115380000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr9:115378600-115380200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr9:115378600-115380200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr9:115378600-115380200	Weak transcription	Esophagus	oesophagus
47	chr9:115378600-115380200	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr9:115378600-115380600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr9:115378600-115380600	Weak transcription	NHDF-Ad	bronchial
50	chr9:115378600-115382800	Weak transcription	Fetal Kidney	kidney

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