Variant report

Variant	nsv1023303
Chromosome Location	chr9:14025605-14286269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2427)
CpG islands
(count:366)
Chromatin interactive
region (count:137)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:16)

(count:2427 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14179625-14179721	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:14213525-14213725	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:14275668-14275697	K562	blood:	n/a	n/a
4	ATF1	chr9:14108004-14108361	K562	blood:	n/a	n/a
5	ATF2	chr9:14251286-14251765	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:14251321-14251781	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr9:14237958-14238821	A549	lung:	n/a	n/a
8	BACH1	chr9:14148860-14148987	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:14156210-14156211	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:14089026-14089193	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr9:14159142-14159209	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr9:14089500-14089693	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:14251353-14251668	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr9:14156185-14156424	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:14247651-14247866	GM12878	blood:	n/a	chr9:14247808-14247817
16	BCL3	chr9:14237978-14238747	A549	lung:	n/a	chr9:14238712-14238721
17	BHLHE40	chr9:14277211-14277493	A549	lung:	n/a	n/a
18	BHLHE40	chr9:14277225-14277603	K562	blood:	n/a	n/a
19	BHLHE40	chr9:14271362-14271562	K562	blood:	n/a	n/a
20	BHLHE40	chr9:14108026-14108352	K562	blood:	n/a	n/a
21	BRCA1	chr9:14031401-14031446	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr9:14178829-14178846	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr9:14030313-14031001	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr9:14142191-14142474	K562	blood:	n/a	n/a
25	CEBPB	chr9:14128066-14128376	IMR90	lung:	n/a	chr9:14128211-14128222
26	CEBPB	chr9:14124200-14124403	A549	lung:	n/a	n/a
27	CEBPB	chr9:14170904-14171247	A549	lung:	n/a	n/a
28	CEBPB	chr9:14080094-14080286	A549	lung:	n/a	n/a
29	CEBPB	chr9:14137010-14137338	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr9:14030339-14030717	MCF-7	breast:	n/a	chr9:14030529-14030540
31	CEBPB	chr9:14086326-14086526	K562	blood:	n/a	chr9:14086457-14086468
32	CEBPB	chr9:14243929-14244165	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:14165711-14166096	ECC-1	luminal epithelium:	n/a	chr9:14165924-14165935
34	CEBPB	chr9:14205407-14205944	A549	lung:	n/a	chr9:14205641-14205653
35	CEBPB	chr9:14184083-14184433	IMR90	lung:	n/a	chr9:14184256-14184267
36	CEBPB	chr9:14096509-14096791	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr9:14159871-14160166	A549	lung:	n/a	chr9:14160037-14160048
38	CEBPB	chr9:14205502-14205868	IMR90	lung:	n/a	chr9:14205641-14205653
39	CEBPB	chr9:14263719-14263934	A549	lung:	n/a	n/a
40	CEBPB	chr9:14238001-14239111	A549	lung:	n/a	n/a
41	CEBPB	chr9:14165742-14166077	Hela-S3	cervix:	n/a	chr9:14165924-14165935
42	CEBPB	chr9:14030340-14030697	ECC-1	luminal epithelium:	n/a	chr9:14030529-14030540
43	CEBPB	chr9:14100584-14100790	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr9:14128051-14128353	K562	blood:	n/a	chr9:14128211-14128222
45	CEBPB	chr9:14035180-14035406	IMR90	lung:	n/a	chr9:14035250-14035261 chr9:14035250-14035263
46	CEBPB	chr9:14215700-14216044	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr9:14238091-14239012	A549	lung:	n/a	n/a
48	CEBPB	chr9:14030336-14030794	ECC-1	luminal epithelium:	n/a	chr9:14030529-14030540
49	CEBPB	chr9:14184163-14184357	H1-hESC	embryonic stem cell:	n/a	chr9:14184256-14184267
50	CEBPB	chr9:14043361-14043685	ECC-1	luminal epithelium:	n/a	n/a

(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	SKMC	muscle:	n/a
2	chr9:14063065-14063115	AG10803	skin:	n/a
3	chr9:14159600-14159650	HNPCEpiC	eye:	n/a
4	chr9:14238640-14238690	AG04450	lung:	fetal
5	chr9:14280660-14280710	PFSK-1	brain:	n/a
6	chr9:14238640-14238690	Jurkat	blood:	n/a
7	chr9:14280660-14280710	AG10803	skin:	n/a
8	chr9:14280660-14280710	BE2_C	brain:	n/a
9	chr9:14159600-14159650	H1-hESC	embryonic stem cell:	embryo
10	chr9:14082328-14082378	HRE	kidney:	n/a
11	chr9:14159600-14159650	HEEpiC	esophagus:	n/a
12	chr9:14082328-14082378	NT2-D1	testis:	n/a
13	chr9:14280660-14280710	H1-hESC	embryonic stem cell:	embryo
14	chr9:14280660-14280710	HepG2	liver:	n/a
15	chr9:14081508-14081558	AG09319	gingival:	n/a
16	chr9:14081508-14081558	T-47D	breast:	n/a
17	chr9:14159600-14159650	NHDF-neo	bronchial:	n/a
18	chr9:14280660-14280710	HEEpiC	esophagus:	n/a
19	chr9:14082328-14082378	GM12892	blood:	n/a
20	chr9:14082328-14082378	HRPEpiC	eye:	n/a
21	chr9:14280660-14280710	GM19239	blood:	n/a
22	chr9:14238640-14238690	BE2_C	brain:	n/a
23	chr9:14159600-14159650	RPTEC	kidney:	n/a
24	chr9:14159600-14159650	Jurkat	blood:	n/a
25	chr9:14081508-14081558	MCF-7	breast:	n/a
26	chr9:14081508-14081558	PrEC	prostate:	n/a
27	chr9:14238640-14238690	HL-60	blood:	n/a
28	chr9:14063065-14063115	HCF	heart:	n/a
29	chr9:14063065-14063115	MCF10A-Er-Src	breast:	n/a
30	chr9:14159600-14159650	MCF10A-Er-Src	breast:	n/a
31	chr9:14159600-14159650	AG10803	skin:	n/a
32	chr9:14280660-14280710	MCF-7	breast:	n/a
33	chr9:14082328-14082378	NHDF-neo	bronchial:	n/a
34	chr9:14081508-14081558	SK-N-SH_RA	brain:	n/a
35	chr9:14063065-14063115	BJ	skin:	n/a
36	chr9:14280660-14280710	HRCEpiC	kidney:	n/a
37	chr9:14159600-14159650	NT2-D1	testis:	n/a
38	chr9:14081508-14081558	HIPEpiC	eye:	n/a
39	chr9:14081508-14081558	AG04449	skin:	fetal
40	chr9:14081508-14081558	H1-hESC	embryonic stem cell:	embryo
41	chr9:14082328-14082378	AG10803	skin:	n/a
42	chr9:14159600-14159650	HL-60	blood:	n/a
43	chr9:14280660-14280710	K562	blood:	n/a
44	chr9:14081508-14081558	SAEC	small airway:	n/a
45	chr9:14081508-14081558	AG04450	lung:	fetal
46	chr9:14082328-14082378	SK-N-SH	brain:	n/a
47	chr9:14280660-14280710	GM12892	blood:	n/a
48	chr9:14082328-14082378	NH-A	brain:	n/a
49	chr9:14159600-14159650	HepG2	liver:	n/a
50	chr9:14082328-14082378	HepG2	liver:	n/a

(count:137 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:14081334..14082892-chr9:14085086..14086767,2	MCF-7	breast:
2	chr9:14081509..14084690-chr9:14096320..14100204,3	MCF-7	breast:
3	chr9:14152718..14156073-chr9:14313268..14315802,3	MCF-7	breast:
4	chr9:14087200..14091584-chr9:14091633..14096199,6	MCF-7	breast:
5	chr9:14261603..14262405-chr9:14406740..14407247,3	MCF-7	breast:
6	chr9:14215028..14217662-chr9:14219597..14221108,2	K562	blood:
7	chr9:14063150..14065584-chr9:14071973..14075080,3	K562	blood:
8	chr9:14131132..14132855-chr9:14133037..14134581,2	MCF-7	breast:
9	chr9:14270274..14272332-chr9:14313445..14314980,2	K562	blood:
10	chr9:14163618..14165126-chr9:14226393..14229305,2	K562	blood:
11	chr9:14117034..14118965-chr9:14313015..14315569,2	MCF-7	breast:
12	chr9:14207609..14210437-chr9:14312286..14315152,2	MCF-7	breast:
13	chr9:14200461..14204358-chr9:14312033..14315867,4	MCF-7	breast:
14	chr9:14097652..14100494-chr9:14313670..14316038,2	MCF-7	breast:
15	chr9:14025076..14027814-chr9:14030099..14033477,4	K562	blood:
16	chr9:14103393..14105851-chr9:14320231..14322166,2	MCF-7	breast:
17	chr9:14239275..14240780-chr9:14249848..14252251,2	MCF-7	breast:
18	chr9:14203657..14206657-chr9:14311874..14315004,3	MCF-7	breast:
19	chr9:14185623..14188206-chr9:14197745..14200671,2	MCF-7	breast:
20	chr9:14207480..14210173-chr9:14216530..14218374,2	MCF-7	breast:
21	chr9:14079254..14081862-chr9:14096417..14098493,2	MCF-7	breast:
22	chr9:14257197..14261472-chr9:14269908..14272185,3	MCF-7	breast:
23	chr9:14249968..14256064-chr9:14312661..14317512,12	MCF-7	breast:
24	chr9:14272688..14274248-chr9:14278922..14280756,2	MCF-7	breast:
25	chr9:14250809..14252545-chr9:14321944..14323813,2	MCF-7	breast:
26	chr9:14185623..14188206-chr9:14197745..14200671,2	MCF-7	breast:
27	chr9:14269033..14270818-chr9:14320491..14322690,2	K562	blood:
28	chr9:14044509..14047236-chr9:14058314..14059901,2	K562	blood:
29	chr9:14030163..14032751-chr9:14052539..14055121,2	MCF-7	breast:
30	chr9:14084996..14087351-chr9:14092569..14095116,2	K562	blood:
31	chr9:14087200..14091584-chr9:14091633..14096199,6	MCF-7	breast:
32	chr9:14265870..14269043-chr9:14313113..14315544,3	MCF-7	breast:
33	chr9:14261603..14262405-chr9:14406659..14407247,4	MCF-7	breast:
34	chr9:14113579..14115515-chr9:14314647..14317550,2	MCF-7	breast:
35	chr9:14129327..14131170-chr9:14138770..14141769,2	K562	blood:
36	chr9:14215028..14217662-chr9:14219597..14221108,2	K562	blood:
37	chr9:14213715..14216528-chr9:14218687..14222056,3	K562	blood:
38	chr9:14163618..14165126-chr9:14226393..14229305,2	K562	blood:
39	chr9:14137259..14139020-chr9:14141233..14143337,2	MCF-7	breast:
40	chr9:14231565..14234116-chr9:14237847..14240047,2	MCF-7	breast:
41	chr9:14228943..14231168-chr9:14236666..14238906,2	MCF-7	breast:
42	chr13:40007058..40008578-chr9:14244599..14246120,2	MCF-7	breast:
43	chr9:14182648..14184578-chr9:14311573..14313374,2	K562	blood:
44	chr9:14135764..14138291-chr9:14312357..14314821,2	MCF-7	breast:
45	chr9:14160671..14162926-chr9:14313281..14316078,2	MCF-7	breast:
46	chr9:14063150..14065584-chr9:14071973..14075080,3	K562	blood:
47	chr9:14030303..14032215-chr9:14033410..14035671,2	K562	blood:
48	chr9:14149670..14153265-chr9:14153637..14156329,3	MCF-7	breast:
49	chr9:14179037..14181363-chr9:14186626..14189533,2	K562	blood:
50	chr9:14228943..14231168-chr9:14236666..14238906,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf146-1	chr9:14026943-14027108	XLOC_007286
2	lnc-C9orf146-1	chr9:14025970-14026076	XLOC_007286
3	lnc-C9orf146-1	chr9:14025969-14026076	NONHSAT130240
4	lnc-ZDHHC21-5	chr9:14081848-14082201	NONHSAT130242
5	lnc-C9orf146-1	chr9:14029951-14030114	NONHSAT130240
6	lnc-C9orf146-1	chr9:14029952-14030114	XLOC_007286
7	lnc-C9orf146-1	chr9:14026942-14027108	NONHSAT130240

No data

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

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

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

Extended variants
information (count: 11071 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:11071 , 50 per page) page: 1 2 3 4 5 6 7 ... 222

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188794224	chr9:14025619-14025620	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs193035094	chr9:14025636-14025637	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs117503827	chr9:14025698-14025699	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs16931255	chr9:14025710-14025711	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs568957105	chr9:14025714-14025715	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs374978169	chr9:14025724-14025725	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs199830098	chr9:14025729-14025730	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs537669966	chr9:14025746-14025747	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs184486054	chr9:14025760-14025761	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs188522974	chr9:14025762-14025763	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs142689134	chr9:14025816-14025817	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs115094145	chr9:14025830-14025831	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs536960213	chr9:14025851-14025852	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs553340550	chr9:14025865-14025866	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs572920594	chr9:14025915-14025916	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs538616053	chr9:14025918-14025919	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs558663526	chr9:14025919-14025920	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs575314103	chr9:14025938-14025939	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs566813261	chr9:14025941-14025942	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs544051324	chr9:14025954-14025955	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs561129323	chr9:14025956-14025957	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs574508528	chr9:14025960-14025961	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs540524526	chr9:14025962-14025963	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs560161045	chr9:14025968-14025969	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs532179643	chr9:14025974-14025975	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs552180870	chr9:14025976-14025977	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs556004909	chr9:14025977-14025978	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs562618281	chr9:14025978-14025979	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs71321958	chr9:14025990-14025991	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs531423324	chr9:14025994-14025995	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs181274772	chr9:14026003-14026004	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs567848880	chr9:14026009-14026010	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs536414126	chr9:14026021-14026022	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs144423002	chr9:14026025-14026026	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs17279781	chr9:14026033-14026034	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs538678266	chr9:14026075-14026076	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs10810079	chr9:14026076-14026077	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs10810080	chr9:14026089-14026090	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs538347951	chr9:14026108-14026109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374736803	chr9:14026113-14026114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147986357	chr9:14026168-14026169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10810081	chr9:14026183-14026184	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs538964865	chr9:14026205-14026206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551225471	chr9:14026263-14026264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141656863	chr9:14026277-14026278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150538026	chr9:14026286-14026287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563016338	chr9:14026331-14026332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545854222	chr9:14026368-14026369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183572660	chr9:14026369-14026370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576266344	chr9:14026384-14026385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	21215367	CNVD

Chromatin state (count:6048 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13994000-14027000	Weak transcription	Aorta	Aorta
2	chr9:14014000-14027000	Weak transcription	Right Atrium	heart
3	chr9:14015400-14027000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr9:14020600-14026800	Weak transcription	Fetal Heart	heart
5	chr9:14022600-14026600	Weak transcription	HUVEC	blood vessel
6	chr9:14022600-14026800	Weak transcription	Fetal Lung	lung
7	chr9:14022800-14028200	Weak transcription	Hela-S3	cervix
8	chr9:14023200-14029400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr9:14024600-14027000	Weak transcription	Left Ventricle	heart
10	chr9:14025000-14026800	Weak transcription	Psoas Muscle	Psoas
11	chr9:14025000-14027000	Weak transcription	Esophagus	oesophagus
12	chr9:14025600-14029800	Weak transcription	Right Ventricle	heart
13	chr9:14026600-14027800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr9:14026600-14028400	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr9:14026600-14029800	Enhancers	HUVEC	blood vessel
16	chr9:14026800-14027000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
17	chr9:14026800-14027200	Enhancers	Fetal Kidney	kidney
18	chr9:14026800-14027400	Enhancers	Colonic Mucosa	Colon
19	chr9:14026800-14027400	Enhancers	Small Intestine	intestine
20	chr9:14026800-14027600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr9:14026800-14027800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr9:14026800-14027800	Enhancers	Adipose Nuclei	Adipose
23	chr9:14026800-14028000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr9:14026800-14028400	Enhancers	Fetal Lung	lung
25	chr9:14026800-14028600	Enhancers	Liver	Liver
26	chr9:14026800-14028600	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr9:14026800-14028800	Enhancers	Psoas Muscle	Psoas
28	chr9:14026800-14029000	Enhancers	Fetal Heart	heart
29	chr9:14027000-14027400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr9:14027000-14027400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr9:14027000-14027400	Enhancers	Esophagus	oesophagus
32	chr9:14027000-14027400	Enhancers	Fetal Intestine Large	intestine
33	chr9:14027000-14027400	Enhancers	Gastric	stomach
34	chr9:14027000-14027400	Enhancers	Left Ventricle	heart
35	chr9:14027000-14027400	Enhancers	Lung	lung
36	chr9:14027000-14027400	Enhancers	Pancreas	Pancrea
37	chr9:14027000-14027400	Enhancers	Stomach Mucosa	stomach
38	chr9:14027000-14027600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr9:14027000-14027800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr9:14027000-14027800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr9:14027000-14027800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr9:14027000-14027800	Enhancers	Muscle Satellite Cultured Cells	--
43	chr9:14027000-14027800	Enhancers	Aorta	Aorta
44	chr9:14027000-14027800	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr9:14027000-14027800	Enhancers	Right Atrium	heart
46	chr9:14027000-14027800	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr9:14027000-14028000	Enhancers	Fetal Muscle Leg	muscle
48	chr9:14027000-14028000	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr9:14027000-14028600	Enhancers	Fetal Intestine Small	intestine
50	chr9:14027000-14028800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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