Variant report

Variant	nsv1017041
Chromosome Location	chr9:674129-860810
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2686)
CpG islands
(count:1283)
Chromatin interactive
region (count:75)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:2686 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:764021-764430	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:734845-735045	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:716213-716255	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:792615-792973	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:755679-756377	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:673768-674544	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:745817-746038	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:706038-706477	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:744770-744894	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:706757-707182	HepG2	liver:	n/a	chr9:706927-706943
11	ARID3A	chr9:710020-710338	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:676651-678350	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:726050-726236	HepG2	liver:	n/a	n/a
14	ARID3A	chr9:682346-683925	HepG2	liver:	n/a	n/a
15	ARID3A	chr9:696723-696891	HepG2	liver:	n/a	n/a
16	ARID3A	chr9:685087-685396	HepG2	liver:	n/a	n/a
17	ATF2	chr9:840342-840725	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr9:859161-859692	GM12878	blood:	n/a	n/a
19	ATF2	chr9:859288-859680	GM12878	blood:	n/a	n/a
20	BACH1	chr9:841437-841715	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr9:801698-801802	H1-hESC	embryonic stem cell:	n/a	chr9:801716-801730
22	BACH1	chr9:674115-674612	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr9:706737-707111	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr9:755709-756109	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
25	BATF	chr9:800791-801012	GM12878	blood:	n/a	n/a
26	BATF	chr9:847470-847844	GM12878	blood:	n/a	n/a
27	BATF	chr9:847504-847840	GM12878	blood:	n/a	n/a
28	BATF	chr9:808690-808887	GM12878	blood:	n/a	n/a
29	BATF	chr9:755733-756053	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
30	BCL11A	chr9:859287-859598	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:674131-674488	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL11A	chr9:859277-859643	GM12878	blood:	n/a	n/a
33	BCL11A	chr9:674204-674357	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL11A	chr9:808677-809119	GM12878	blood:	n/a	n/a
35	BCL11A	chr9:840410-840568	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL3	chr9:694616-695281	A549	lung:	n/a	n/a
37	BHLHE40	chr9:755691-756354	HepG2	liver:	n/a	n/a
38	BHLHE40	chr9:682578-683474	HepG2	liver:	n/a	n/a
39	BHLHE40	chr9:852632-852864	GM12878	blood:	n/a	n/a
40	BHLHE40	chr9:859004-859714	GM12878	blood:	n/a	n/a
41	BHLHE40	chr9:734758-735070	HepG2	liver:	n/a	n/a
42	BHLHE40	chr9:761513-761762	HepG2	liver:	n/a	n/a
43	BHLHE40	chr9:706697-706897	GM12878	blood:	n/a	n/a
44	BHLHE40	chr9:694893-695215	A549	lung:	n/a	n/a
45	BHLHE40	chr9:682623-683064	HepG2	liver:	n/a	n/a
46	BRCA1	chr9:756272-756352	HepG2	liver:	n/a	n/a
47	BRCA1	chr9:763966-764464	H1-hESC	embryonic stem cell:	n/a	n/a
48	CBX3	chr9:763894-764606	HCT-116	colon:	n/a	n/a
49	CEBPB	chr9:756000-756376	K562	blood:	n/a	chr9:756184-756197 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195
50	CEBPB	chr9:799183-799446	HepG2	liver:	n/a	chr9:799301-799312

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:714269-714319	Jurkat	blood:	n/a
2	chr9:826657-826707	AG09309	skin:	n/a
3	chr9:714269-714319	Jurkat	blood:	n/a
4	chr9:826657-826707	AG09309	skin:	n/a
5	chr9:843179-843229	AG09319	gingival:	n/a
6	chr9:839557-839607	Jurkat	blood:	n/a
7	chr9:841436-841486	HepG2	liver:	n/a
8	chr9:707387-707437	HRCEpiC	kidney:	n/a
9	chr9:841850-841900	T-47D	breast:	n/a
10	chr9:705143-705193	GM19239	blood:	n/a
11	chr9:842914-842964	ECC-1	luminal epithelium:	n/a
12	chr9:841632-841682	GM19239	blood:	n/a
13	chr9:841850-841900	GM12892	blood:	n/a
14	chr9:761482-761532	AoSMC	blood vessel:	n/a
15	chr9:714269-714319	HCM	heart:	n/a
16	chr9:841436-841486	AG09309	skin:	n/a
17	chr9:842914-842964	HCM	heart:	n/a
18	chr9:761482-761532	HCF	heart:	n/a
19	chr9:843179-843229	HMEC	breast:	n/a
20	chr9:826657-826707	IMR90	lung:	fetal
21	chr9:843179-843229	GM12891	blood:	n/a
22	chr9:707387-707437	CMK	blood:	n/a
23	chr9:842914-842964	LNCaP	prostate:	n/a
24	chr9:841636-841686	GM06990	blood:	n/a
25	chr9:841850-841900	NHBE	bronchial:	n/a
26	chr9:841850-841900	ovcar-3	ovarian:	n/a
27	chr9:707410-707460	ECC-1	luminal epithelium:	n/a
28	chr9:842799-842849	RPTEC	kidney:	n/a
29	chr9:707410-707460	NHBE	bronchial:	n/a
30	chr9:842799-842849	AG09309	skin:	n/a
31	chr9:707387-707437	HUVEC	blood vessel:	n/a
32	chr9:841636-841686	ovcar-3	ovarian:	n/a
33	chr9:761482-761532	AG04449	skin:	fetal
34	chr9:857563-857613	HRE	kidney:	n/a
35	chr9:839557-839607	NH-A	brain:	n/a
36	chr9:841340-841390	BE2_C	brain:	n/a
37	chr9:761482-761532	K562	blood:	n/a
38	chr9:842914-842964	HL-60	blood:	n/a
39	chr9:841636-841686	ECC-1	luminal epithelium:	n/a
40	chr9:714269-714319	K562	blood:	n/a
41	chr9:857563-857613	Caco-2	colon:	n/a
42	chr9:714269-714319	NB4	blood:	n/a
43	chr9:839557-839607	HRPEpiC	eye:	n/a
44	chr9:842799-842849	HRE	kidney:	n/a
45	chr9:839557-839607	HPAEpiC	pulmonary alveolar:	n/a
46	chr9:839557-839607	HMEC	breast:	n/a
47	chr9:826657-826707	PFSK-1	brain:	n/a
48	chr9:705143-705193	Hepatocyte	liver:	n/a
49	chr9:707410-707460	GM06990	blood:	n/a
50	chr9:841636-841686	GM12892	blood:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
2	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
3	chr9:706377..708156-chr9:805249..808005,2	MCF-7	breast:
4	chr9:846543..848941-chr9:858349..860587,2	K562	blood:
5	chr9:763806..764607-chr9:806256..807153,5	MCF-7	breast:
6	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
7	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
8	chr9:686763..689090-chr9:692801..694616,2	MCF-7	breast:
9	chr9:385566..386417-chr9:764222..764740,2	MCF-7	breast:
10	chr9:719690..721572-chr9:723182..726115,2	MCF-7	breast:
11	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
12	chr9:707320..708881-chr9:710200..712479,2	MCF-7	breast:
13	chr9:697287..699295-chr9:705065..707332,2	K562	blood:
14	chr9:613348..614490-chr9:763793..765061,13	MCF-7	breast:
15	chr9:725965..727738-chr9:729421..731068,2	MCF-7	breast:
16	chr9:710784..713169-chr9:756222..759004,2	MCF-7	breast:
17	chr9:757453..760203-chr9:763946..765702,2	MCF-7	breast:
18	chr9:707320..708881-chr9:710200..712479,2	MCF-7	breast:
19	chr9:682966..685572-chr9:709711..712587,2	MCF-7	breast:
20	chr9:782884..784766-chr9:785783..787661,2	MCF-7	breast:
21	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
22	chr9:826413..827016-chr9:1004866..1005745,2	MCF-7	breast:
23	chr9:706307..708254-chr9:737100..740465,4	MCF-7	breast:
24	chr9:691921..694076-chr9:697704..699992,2	K562	blood:
25	chr9:763806..764607-chr9:806256..807153,5	MCF-7	breast:
26	chr9:744945..746598-chr9:748652..750929,2	K562	blood:
27	chr9:846543..848941-chr9:858349..860587,2	K562	blood:
28	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
29	chr9:719690..721572-chr9:723182..726115,2	MCF-7	breast:
30	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
31	chr9:721333..724004-chr9:738366..740594,2	MCF-7	breast:
32	chr9:858181..863479-chr9:867333..871768,4	MCF-7	breast:
33	chr9:721333..724004-chr9:738366..740594,2	MCF-7	breast:
34	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
35	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
36	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:
37	chr9:843269..845393-chr9:851272..854140,2	MCF-7	breast:
38	chr9:705245..708353-chr9:743847..747461,3	MCF-7	breast:
39	chr9:704209..707068-chr9:719899..721523,2	MCF-7	breast:
40	chr9:829461..831177-chr9:832230..834782,2	MCF-7	breast:
41	chr9:707080..708925-chr9:715815..718212,3	MCF-7	breast:
42	chr9:782884..784766-chr9:785783..787661,2	MCF-7	breast:
43	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
44	chr9:829461..831177-chr9:832230..834782,2	MCF-7	breast:
45	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
46	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
47	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
48	chr9:707080..708925-chr9:715815..718212,3	MCF-7	breast:
49	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
50	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf66-3	chr9:673817-674379	ENSG00000227914.1
2	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.1
3	lnc-C9orf66-4	chr9:761299-761551	XLOC_007628
4	lnc-C9orf66-5	chr9:755232-755507	XLOC_007629
5	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.1
6	lnc-C9orf66-5	chr9:752722-752856	XLOC_007629
7	lnc-C9orf66-4	chr9:749336-749509	XLOC_007628
8	lnc-C9orf66-4	chr9:749336-749496	XLOC_007628
9	lnc-C9orf66-4	chr9:747413-747469	XLOC_007628
10	lnc-C9orf66-3	chr9:674124-674379	ENSG00000227914.3
11	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.3
12	lnc-KANK1-1	chr9:747412-747469	NONHSAT129937
13	lnc-KANK1-1	chr9:748000-751056	NONHSAT129937
14	lnc-C9orf66-3	chr9:677542-677628	ENSG00000227914.3
15	lnc-KANK1-1	chr9:747272-747365	NONHSAT129937
16	lnc-C9orf66-4	chr9:747413-747469	XLOC_007628
17	lnc-KANK1-1	chr9:746431-746497	NONHSAT129937
18	lnc-C9orf66-3	chr9:673478-674379	ENSG00000227914.3
19	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.3

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	KANK1	hsa-miR-335-5p	chr9:746085-746104
2	KANK1	hsa-miR-124-3p	chr9:746055-746062
3	KANK1	hsa-miR-10a-5p	chr9:745092-745115
4	KANK1	hsa-miR-335-5p	chr9:746049-746071
5	KANK1	hsa-miR-124-3p	chr9:746043-746062

Variant related genes	Relation type
ENSG00000227914	TF binding region
KANK1	TF binding region
DMRT1	TF binding region
ENSG00000227914	CpG island
KANK1	CpG island
DMRT1	CpG island
ENSG00000227914	chromatin interactions
ENSG00000107104	chromatin interactions
ENSG00000108557	chromatin interactions
PPM1A	miRNA target sites
FAM123B	miRNA target sites
SOD2	miRNA target sites

Extended variants
information (count: 9232 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:9232 , 50 per page) page: 1 2 3 4 5 6 7 ... 185

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554222810	chr9:674137-674138	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
2	rs567948009	chr9:674183-674184	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs138821078	chr9:674217-674218	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs11791986	chr9:674275-674276	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs16922321	chr9:674298-674299	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs189052761	chr9:674324-674325	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
7	rs530475474	chr9:674341-674342	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
8	rs371713514	chr9:674352-674353	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
9	rs553296670	chr9:674364-674365	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
10	rs543921701	chr9:674382-674383	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs61067104	chr9:674383-674384	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs113738657	chr9:674385-674386	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs572636747	chr9:674386-674387	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs148018459	chr9:674400-674401	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs149433964	chr9:674401-674402	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs79471487	chr9:674403-674404	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs562146230	chr9:674411-674412	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs531167713	chr9:674414-674415	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs4742217	chr9:674428-674429	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs564637334	chr9:674461-674462	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs16922323	chr9:674467-674468	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs551911450	chr9:674503-674504	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs114524702	chr9:674512-674513	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs373404189	chr9:674528-674529	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs138185334	chr9:674577-674578	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs375539240	chr9:674581-674582	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs567813570	chr9:674597-674598	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs149585448	chr9:674669-674670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs34810617	chr9:674672-674673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs62531168	chr9:674674-674675	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs371812635	chr9:674707-674708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532448213	chr9:674735-674736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552970377	chr9:674739-674740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573306295	chr9:674760-674761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535838229	chr9:674779-674780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555941095	chr9:674784-674785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs55680746	chr9:674789-674790	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs182442779	chr9:674828-674829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564677338	chr9:674837-674838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186311173	chr9:674846-674847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs578096002	chr9:674857-674858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11792599	chr9:674863-674864	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs560613603	chr9:674870-674871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528124336	chr9:674891-674892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189097606	chr9:674911-674912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557644474	chr9:674916-674917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530487400	chr9:674922-674923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571071317	chr9:674930-674931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570653257	chr9:674953-674954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10758802	chr9:674954-674955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance

Variant related diseases (count:115)

Disease	PMID	Source
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	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
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
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
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-small cell lung cancer	16651412	CNVD
Cancer	21272361	CNVD
Schizophrenia	20967226	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:4873 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:653400-698000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:670800-675800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr9:670800-675800	Weak transcription	Esophagus	oesophagus
4	chr9:670800-677200	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr9:670800-677600	Weak transcription	Gastric	stomach
6	chr9:670800-706800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:672000-674200	Enhancers	Brain Cingulate Gyrus	brain
8	chr9:672000-674600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr9:672000-674600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr9:672000-674600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr9:672000-675000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr9:672000-676600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr9:672000-676800	Enhancers	HepG2	liver
14	chr9:672000-677000	Enhancers	HMEC	breast
15	chr9:672000-677200	Enhancers	Brain Hippocampus Middle	brain
16	chr9:672200-674600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr9:672200-676600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr9:672400-674600	Enhancers	Brain Substantia Nigra	brain
19	chr9:673000-674200	Enhancers	Stomach Mucosa	stomach
20	chr9:673000-674400	Enhancers	Liver	Liver
21	chr9:673000-674600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:673200-674200	Enhancers	Right Atrium	heart
23	chr9:673200-674400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr9:673200-674400	Enhancers	Brain Angular Gyrus	brain
25	chr9:673200-674400	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr9:673200-674400	Enhancers	Left Ventricle	heart
27	chr9:673200-677400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr9:673400-674400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:673400-674400	Enhancers	Colon Smooth Muscle	Colon
30	chr9:673400-674600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr9:673600-674200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr9:673600-674200	Enhancers	Brain Germinal Matrix	brain
33	chr9:673600-674400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr9:673600-674400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr9:673600-674400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr9:673600-674400	Enhancers	Adipose Nuclei	Adipose
37	chr9:673600-674400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr9:673600-674400	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr9:673600-674600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr9:673600-674600	Enhancers	Fetal Intestine Small	intestine
41	chr9:673600-674600	Enhancers	Rectal Smooth Muscle	rectum
42	chr9:673600-674800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr9:673600-675000	Enhancers	H1 Cell Line	embryonic stem cell
44	chr9:673600-677800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr9:673600-677800	Weak transcription	Pancreas	Pancrea
46	chr9:673800-674200	Enhancers	Fetal Heart	heart
47	chr9:673800-674200	Enhancers	Stomach Smooth Muscle	stomach
48	chr9:673800-674400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:673800-674400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr9:673800-674400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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