Variant report

Variant	nsv1033764
Chromosome Location	chr9:13764918-14226168
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2539)
CpG islands
(count:366)
Chromatin interactive
region (count:116)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:16)

(count:2539 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14213525-14213725	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:14179625-14179721	HepG2	liver:	n/a	n/a
3	ATF1	chr9:14108004-14108361	K562	blood:	n/a	n/a
4	BACH1	chr9:14156210-14156211	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:14148860-14148987	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:13970161-13970279	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:14159142-14159209	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:14089026-14089193	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr9:14089500-14089693	GM12878	blood:	n/a	n/a
10	BATF	chr9:13967560-13967810	GM12878	blood:	n/a	n/a
11	BATF	chr9:13963058-13963287	GM12878	blood:	n/a	chr9:13963123-13963134
12	BATF	chr9:13967555-13967818	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:13967599-13967799	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:14156185-14156424	GM12878	blood:	n/a	n/a
15	BHLHE40	chr9:14108026-14108352	K562	blood:	n/a	n/a
16	BRCA1	chr9:14031401-14031446	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr9:14178829-14178846	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr9:13901062-13901120	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr9:14030313-14031001	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr9:13942597-13943057	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr9:14142191-14142474	K562	blood:	n/a	n/a
22	CEBPB	chr9:14096493-14096875	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr9:14036025-14036269	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:13979521-13979870	A549	lung:	n/a	chr9:13979716-13979729 chr9:13979674-13979685 chr9:13979685-13979696
25	CEBPB	chr9:14184081-14184424	HepG2	liver:	n/a	chr9:14184256-14184267
26	CEBPB	chr9:14215550-14216153	A549	lung:	n/a	n/a
27	CEBPB	chr9:13860100-13860471	HepG2	liver:	n/a	chr9:13860281-13860292
28	CEBPB	chr9:13806756-13807094	Hela-S3	cervix:	n/a	chr9:13806926-13806937 chr9:13806958-13806969
29	CEBPB	chr9:14165927-14165989	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr9:14188121-14188244	HepG2	liver:	n/a	chr9:14188196-14188207 chr9:14188196-14188209 chr9:14188198-14188209 chr9:14188196-14188209
31	CEBPB	chr9:14128066-14128376	IMR90	lung:	n/a	chr9:14128211-14128222
32	CEBPB	chr9:13949782-13949932	A549	lung:	n/a	n/a
33	CEBPB	chr9:14215666-14216071	IMR90	lung:	n/a	n/a
34	CEBPB	chr9:14222198-14222504	H1-hESC	embryonic stem cell:	n/a	chr9:14222335-14222352
35	CEBPB	chr9:14184145-14184422	Hela-S3	cervix:	n/a	chr9:14184256-14184267
36	CEBPB	chr9:14030339-14030717	MCF-7	breast:	n/a	chr9:14030529-14030540
37	CEBPB	chr9:14205502-14205868	IMR90	lung:	n/a	chr9:14205641-14205653
38	CEBPB	chr9:14043361-14043685	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr9:14221536-14221962	MCF-7	breast:	n/a	chr9:14221755-14221768
40	CEBPB	chr9:14086326-14086526	K562	blood:	n/a	chr9:14086457-14086468
41	CEBPB	chr9:14221242-14221954	A549	lung:	n/a	chr9:14221755-14221768
42	CEBPB	chr9:14184102-14184384	K562	blood:	n/a	chr9:14184256-14184267
43	CEBPB	chr9:14173196-14173425	A549	lung:	n/a	chr9:14173346-14173357
44	CEBPB	chr9:13806750-13807116	HepG2	liver:	n/a	chr9:13806926-13806937 chr9:13806958-13806969
45	CEBPB	chr9:14221397-14222104	A549	lung:	n/a	chr9:14221755-14221768
46	CEBPB	chr9:13817804-13818135	A549	lung:	n/a	chr9:13817954-13817967 chr9:13817953-13817970
47	CEBPB	chr9:13971110-13971413	A549	lung:	n/a	chr9:13971264-13971275
48	CEBPB	chr9:13817778-13818103	A549	lung:	n/a	chr9:13817954-13817967 chr9:13817953-13817970
49	CEBPB	chr9:13817776-13818148	IMR90	lung:	n/a	chr9:13817954-13817967 chr9:13817953-13817970
50	CEBPB	chr9:14205499-14205786	A549	lung:	n/a	chr9:14205641-14205653

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14082328-14082378	HNPCEpiC	eye:	n/a
2	chr9:13860785-13860835	IMR90	lung:	fetal
3	chr9:14082328-14082378	BE2_C	brain:	n/a
4	chr9:14081508-14081558	HCM	heart:	n/a
5	chr9:13897073-13897123	Hela-S3	cervix:	n/a
6	chr9:14159600-14159650	IMR90	lung:	fetal
7	chr9:13897073-13897123	NHBE	bronchial:	n/a
8	chr9:14063065-14063115	HEEpiC	esophagus:	n/a
9	chr9:14063065-14063115	LNCaP	prostate:	n/a
10	chr9:13897073-13897123	PANC-1	pancreas:	n/a
11	chr9:14063065-14063115	HCPEpiC	choroid plexus:	n/a
12	chr9:14063065-14063115	SK-N-MC	brain:	n/a
13	chr9:13897073-13897123	HRPEpiC	eye:	n/a
14	chr9:13860785-13860835	Hela-S3	cervix:	n/a
15	chr9:14063065-14063115	MCF10A-Er-Src	breast:	n/a
16	chr9:13860785-13860835	PFSK-1	brain:	n/a
17	chr9:14082328-14082378	NB4	blood:	n/a
18	chr9:13897073-13897123	BJ	skin:	n/a
19	chr9:14081508-14081558	AG09309	skin:	n/a
20	chr9:14081508-14081558	PANC-1	pancreas:	n/a
21	chr9:14082328-14082378	AoSMC	blood vessel:	n/a
22	chr9:14082328-14082378	BJ	skin:	n/a
23	chr9:14159600-14159650	AoSMC	blood vessel:	n/a
24	chr9:14063065-14063115	Jurkat	blood:	n/a
25	chr9:14159600-14159650	PANC-1	pancreas:	n/a
26	chr9:13897073-13897123	AG09309	skin:	n/a
27	chr9:14063065-14063115	PFSK-1	brain:	n/a
28	chr9:13897073-13897123	SKMC	muscle:	n/a
29	chr9:13897073-13897123	CMK	blood:	n/a
30	chr9:13897073-13897123	NHDF-neo	bronchial:	n/a
31	chr9:13860785-13860835	HAEpiC	amniotic membrane:	n/a
32	chr9:14159600-14159650	Caco-2	colon:	n/a
33	chr9:14159600-14159650	ECC-1	luminal epithelium:	n/a
34	chr9:13897073-13897123	HEEpiC	esophagus:	n/a
35	chr9:14159600-14159650	Hepatocyte	liver:	n/a
36	chr9:14159600-14159650	LNCaP	prostate:	n/a
37	chr9:14082328-14082378	HCT-116	colon:	n/a
38	chr9:14082328-14082378	NHBE	bronchial:	n/a
39	chr9:14082328-14082378	Hela-S3	cervix:	n/a
40	chr9:14081508-14081558	PrEC	prostate:	n/a
41	chr9:14082328-14082378	PFSK-1	brain:	n/a
42	chr9:14063065-14063115	ovcar-3	ovarian:	n/a
43	chr9:14081508-14081558	Jurkat	blood:	n/a
44	chr9:13897073-13897123	AG04450	lung:	fetal
45	chr9:13897073-13897123	NB4	blood:	n/a
46	chr9:14081508-14081558	ovcar-3	ovarian:	n/a
47	chr9:13860785-13860835	AG09309	skin:	n/a
48	chr9:14081508-14081558	HAEpiC	amniotic membrane:	n/a
49	chr9:14082328-14082378	AG09309	skin:	n/a
50	chr9:14081508-14081558	U87	brain:	n/a

(count:116 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:14179037..14181363-chr9:14186626..14189533,2	K562	blood:
2	chr9:14084490..14087404-chr9:14119723..14122409,2	K562	blood:
3	chr9:14215028..14217662-chr9:14219597..14221108,2	K562	blood:
4	chr9:14180541..14184155-chr9:14313790..14316409,3	MCF-7	breast:
5	chr9:14129327..14131170-chr9:14138770..14141769,2	K562	blood:
6	chr9:14198108..14200232-chr9:14207218..14209041,2	MCF-7	breast:
7	chr9:14087200..14091584-chr9:14091633..14096199,6	MCF-7	breast:
8	chr9:14097652..14100494-chr9:14313670..14316038,2	MCF-7	breast:
9	chr9:13853291..13855822-chr9:13857437..13860542,3	K562	blood:
10	chr9:14044509..14047236-chr9:14058314..14059901,2	K562	blood:
11	chr9:14081509..14084690-chr9:14096320..14100204,3	MCF-7	breast:
12	chr9:14211963..14213596-chr9:14216891..14219507,2	K562	blood:
13	chr9:14071890..14074475-chr9:14076028..14078439,2	MCF-7	breast:
14	chr9:14022228..14025060-chr9:14026998..14028681,2	MCF-7	breast:
15	chr9:14223793..14226601-chr9:14227808..14230396,2	MCF-7	breast:
16	chr9:14220500..14222113-chr9:14225343..14228147,2	MCF-7	breast:
17	chr9:13842636..13844201-chr9:13847494..13849410,2	K562	blood:
18	chr9:14074317..14076748-chr9:14077516..14080431,2	K562	blood:
19	chr9:14063150..14065584-chr9:14071973..14075080,3	K562	blood:
20	chr9:13851030..13853647-chr9:13854118..13856887,2	MCF-7	breast:
21	chr9:14198108..14200232-chr9:14207218..14209041,2	MCF-7	breast:
22	chr9:14107952..14109825-chr9:14313047..14315563,2	MCF-7	breast:
23	chr9:14113579..14115515-chr9:14314647..14317550,2	MCF-7	breast:
24	chr9:14119573..14121369-chr9:14313946..14316559,2	MCF-7	breast:
25	chr9:14007035..14009577-chr9:14012509..14014368,2	MCF-7	breast:
26	chr9:13896594..13899401-chr9:13941918..13943557,2	K562	blood:
27	chr9:14203657..14206657-chr9:14311874..14315004,3	MCF-7	breast:
28	chr9:14182648..14184578-chr9:14311573..14313374,2	K562	blood:
29	chr9:14135764..14138291-chr9:14312357..14314821,2	MCF-7	breast:
30	chr9:14163618..14165126-chr9:14226393..14229305,2	K562	blood:
31	chr9:13977418..13979333-chr9:13982730..13984580,2	K562	blood:
32	chr9:14137259..14139020-chr9:14141233..14143337,2	MCF-7	breast:
33	chr9:13853960..13855766-chr9:13858743..13860340,2	MCF-7	breast:
34	chr9:14137259..14139020-chr9:14141233..14143337,2	MCF-7	breast:
35	chr9:13851030..13853647-chr9:13854118..13856887,2	MCF-7	breast:
36	chr9:14030303..14032215-chr9:14033410..14035671,2	K562	blood:
37	chr9:14200461..14204358-chr9:14312033..14315867,4	MCF-7	breast:
38	chr9:14060071..14062490-chr9:14064444..14067152,2	MCF-7	breast:
39	chr9:14131132..14132855-chr9:14133037..14134581,2	MCF-7	breast:
40	chr9:14149670..14153265-chr9:14153637..14156329,3	MCF-7	breast:
41	chr9:14183906..14185833-chr9:14191618..14193505,2	K562	blood:
42	chr9:14104339..14106002-chr9:14106251..14108537,2	MCF-7	breast:
43	chr9:14129327..14131170-chr9:14138770..14141769,2	K562	blood:
44	chr9:14207480..14210173-chr9:14216530..14218374,2	MCF-7	breast:
45	chr9:13977418..13979333-chr9:13982730..13984580,2	K562	blood:
46	chr9:14171238..14174758-chr9:14313381..14316374,3	MCF-7	breast:
47	chr9:14185623..14188206-chr9:14197745..14200671,2	MCF-7	breast:
48	chr9:14087200..14091584-chr9:14091633..14096199,6	MCF-7	breast:
49	chr9:14183906..14185833-chr9:14191618..14193505,2	K562	blood:
50	chr9:14207609..14210437-chr9:14312286..14315152,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf146-4	chr9:13945391-13945609	ENSG00000205636.3
2	lnc-C9orf146-1	chr9:14025970-14026076	XLOC_007286
3	lnc-C9orf146-4	chr9:13927970-13928060	NR_038194
4	lnc-C9orf146-4	chr9:13945391-13945606	NR_038194
5	lnc-C9orf146-1	chr9:14025969-14026076	NONHSAT130240
6	lnc-C9orf146-5	chr9:14019952-14020114	NONHSAT130239
7	lnc-C9orf146-1	chr9:14026943-14027108	XLOC_007286
8	lnc-C9orf146-4	chr9:13944374-13944450	NR_038194
9	lnc-C9orf146-5	chr9:14016943-14017108	NONHSAT130239
10	lnc-C9orf146-5	chr9:14015970-14016076	NONHSAT130239
11	lnc-NFIB-2	chr9:13929910-13930118	uc_250_-
12	lnc-C9orf150-5	chr9:13929910-13930118	uc_250_+
13	lnc-ZDHHC21-5	chr9:14081848-14082201	NONHSAT130242
14	lnc-C9orf146-4	chr9:13927970-13928060	ENSG00000205636.3
15	lnc-C9orf146-1	chr9:14029951-14030114	NONHSAT130240
16	lnc-C9orf146-4	chr9:13944374-13944450	ENSG00000205636.3
17	lnc-C9orf146-1	chr9:14026942-14027108	NONHSAT130240
18	lnc-C9orf146-1	chr9:14029952-14030114	XLOC_007286

No data

(count:16 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NFIB	hsa-miR-19b-3p	chr9:14086847-14086869
2	NFIB	hsa-miR-19b-3p	chr9:14083381-14083402
3	NFIB	hsa-miR-21-5p	chr9:14082464-14082488
4	NFIB	hsa-miR-124-3p	chr9:14087883-14087877
5	NFIB	hsa-miR-19b-3p	chr9:14086853-14086847
6	NFIB	hsa-miR-92a-3p	chr9:14087425-14087446
7	NFIB	hsa-miR-21-5p	chr9:14087859-14087880
8	NFIB	hsa-miR-124-3p	chr9:14086824-14086818
9	NFIB	hsa-miR-92a-3p	chr9:14086463-14086457
10	NFIB	hsa-miR-93-5p	chr9:14083378-14083400
11	NFIB	hsa-miR-21-5p	chr9:14087865-14087858
12	NFIB	hsa-miR-130b-3p	chr9:14083386-14083380
13	NFIB	hsa-miR-93-5p	chr9:14083384-14083378
14	NFIB	hsa-miR-19b-3p	chr9:14083387-14083381
15	NFIB	hsa-miR-130b-3p	chr9:14083380-14083403
16	NFIB	hsa-miR-92a-3p	chr9:14087431-14087425

Variant related genes	Relation type
PES1P2	TF binding region
NFIB	TF binding region
ENSG00000213954	TF binding region
ENSG00000235533	TF binding region
RPL3P11	TF binding region
ENSG00000234982	TF binding region
LINC00583	TF binding region
PES1P2	CpG island
NFIB	CpG island
ENSG00000213954	CpG island
ENSG00000235533	CpG island
RPL3P11	CpG island
ENSG00000234982	CpG island
LINC00583	CpG island
ENSG00000235533	chromatin interactions
ENSG00000225472	chromatin interactions
ENSG00000147862	chromatin interactions

Extended variants
information (count: 21536 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:21536 , 50 per page) page: 1 2 3 4 5 6 7 ... 431

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555792316	chr9:13764918-13764919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561988366	chr9:13764920-13764921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373768074	chr9:13764928-13764929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547176050	chr9:13764943-13764944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376102912	chr9:13764957-13764958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138950473	chr9:13764977-13764978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570478732	chr9:13764987-13764988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186206929	chr9:13765026-13765027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559158101	chr9:13765047-13765048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575930718	chr9:13765051-13765052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs74572532	chr9:13765085-13765086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555277153	chr9:13765091-13765092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574732337	chr9:13765095-13765096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144726623	chr9:13765100-13765101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201863152	chr9:13765102-13765103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200714699	chr9:13765104-13765105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs398068473	chr9:13765106-13765107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549863137	chr9:13765129-13765130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560295300	chr9:13765184-13765185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191011708	chr9:13765194-13765195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148783004	chr9:13765204-13765205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562322362	chr9:13765205-13765206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12343138	chr9:13765216-13765217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs374537115	chr9:13765234-13765235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548073343	chr9:13765272-13765273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562064737	chr9:13765282-13765283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181956555	chr9:13765287-13765288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547326892	chr9:13765291-13765292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs966992	chr9:13765292-13765293	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs539510698	chr9:13765293-13765294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549928940	chr9:13765295-13765296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569457683	chr9:13765296-13765297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538480929	chr9:13765297-13765298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554960001	chr9:13765298-13765299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575037260	chr9:13765299-13765300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534241570	chr9:13765301-13765302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs966991	chr9:13765312-13765313	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs576855633	chr9:13765332-13765333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142452552	chr9:13765334-13765335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146401283	chr9:13765371-13765372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs966990	chr9:13765376-13765377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs541964070	chr9:13765389-13765390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73650633	chr9:13765390-13765391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568456704	chr9:13765395-13765396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139770892	chr9:13765397-13765398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185738633	chr9:13765419-13765420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76712026	chr9:13765429-13765430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532990805	chr9:13765440-13765441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144183707	chr9:13765445-13765446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569814800	chr9:13765469-13765470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Breast cancer	21611746	CNVD
Schizophrenia	23813976	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Renal cell carcinoma	21215367	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic cancer	17952125	CNVD
Glycine encephalopathy	21572526	CNVD
early-passage human iPS cells	21368824	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	21215367	CNVD

Chromatin state (count:5016 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13758200-13787200	Weak transcription	Aorta	Aorta
2	chr9:13777000-13777400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:13777000-13779600	Enhancers	Fetal Muscle Leg	muscle
4	chr9:13777200-13777600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:13777400-13778800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr9:13777600-13778000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:13778000-13779600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr9:13778000-13779600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr9:13778200-13778600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr9:13778200-13778600	Enhancers	HSMM	muscle
11	chr9:13778200-13778600	Enhancers	HSMMtube	muscle
12	chr9:13778200-13779000	Enhancers	NH-A	brain
13	chr9:13778200-13779800	Enhancers	Fetal Heart	heart
14	chr9:13778400-13779000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:13778600-13779000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr9:13778600-13779000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
17	chr9:13778600-13779000	Flanking Active TSS	HSMM	muscle
18	chr9:13778600-13779200	Flanking Active TSS	HSMMtube	muscle
19	chr9:13778600-13779400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr9:13778800-13779000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr9:13778800-13779000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:13778800-13779400	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr9:13778800-13779400	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr9:13779000-13779400	Enhancers	Muscle Satellite Cultured Cells	--
25	chr9:13779000-13779600	Enhancers	HSMM	muscle
26	chr9:13779000-13791600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:13779200-13779400	Enhancers	HSMMtube	muscle
28	chr9:13779800-13785600	Weak transcription	Fetal Heart	heart
29	chr9:13785600-13787000	Enhancers	Fetal Heart	heart
30	chr9:13785800-13787000	Enhancers	NHLF	lung
31	chr9:13785800-13787200	Enhancers	Fetal Lung	lung
32	chr9:13785800-13787200	Enhancers	Right Ventricle	heart
33	chr9:13785800-13787200	Enhancers	NHDF-Ad	bronchial
34	chr9:13786000-13787000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr9:13786000-13787000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr9:13786000-13787000	Enhancers	Right Atrium	heart
37	chr9:13786000-13787400	Enhancers	Fetal Muscle Leg	muscle
38	chr9:13786200-13786400	Enhancers	Brain Angular Gyrus	brain
39	chr9:13786200-13786400	Enhancers	Brain Cingulate Gyrus	brain
40	chr9:13786200-13786400	Enhancers	Fetal Muscle Trunk	muscle
41	chr9:13786200-13786400	Enhancers	Psoas Muscle	Psoas
42	chr9:13786200-13787000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr9:13786200-13787000	Enhancers	Adipose Nuclei	Adipose
44	chr9:13786200-13787200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr9:13786200-13787200	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr9:13786200-13787200	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr9:13786200-13787200	Enhancers	Stomach Smooth Muscle	stomach
48	chr9:13786200-13787400	Enhancers	HSMMtube	muscle
49	chr9:13786200-13787600	Enhancers	Left Ventricle	heart
50	chr9:13786200-13787600	Enhancers	HSMM	muscle

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