Variant report

Variant	nsv1038467
Chromosome Location	chr12:59680717-59999008
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2194)
CpG islands
(count:1222)
Chromatin interactive
region (count:49)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2194 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:59797100-59797444	HepG2	liver:	n/a	chr12:59797314-59797330
2	ARID3A	chr12:59990012-59990103	HepG2	liver:	n/a	n/a
3	ATF2	chr12:59711326-59712140	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:59990321-59991736	GM12878	blood:	n/a	n/a
5	ATF2	chr12:59715232-59716577	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr12:59991078-59991577	GM12878	blood:	n/a	n/a
7	ATF2	chr12:59712703-59713078	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:59989925-59990860	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr12:59893664-59893893	GM12878	blood:	n/a	n/a
10	BATF	chr12:59893585-59893850	GM12878	blood:	n/a	n/a
11	BATF	chr12:59991262-59991562	GM12878	blood:	n/a	n/a
12	BATF	chr12:59991182-59991631	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:59893631-59893857	GM12878	blood:	n/a	chr12:59893760-59893769
14	BCL3	chr12:59928674-59929037	GM12878	blood:	n/a	n/a
15	BCL3	chr12:59928657-59928995	GM12878	blood:	n/a	n/a
16	BCL3	chr12:59928231-59928552	GM12878	blood:	n/a	n/a
17	BCLAF1	chr12:59990577-59991601	GM12878	blood:	n/a	n/a
18	BCLAF1	chr12:59797005-59797347	GM12878	blood:	n/a	n/a
19	BCLAF1	chr12:59991058-59991596	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:59989349-59991652	GM12878	blood:	n/a	chr12:59990247-59990263 chr12:59990812-59990825 chr12:59989835-59989851
21	BHLHE40	chr12:59801689-59801776	GM12878	blood:	n/a	chr12:59801704-59801713
22	BHLHE40	chr12:59997664-59997902	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:59989927-59991031	HepG2	liver:	n/a	chr12:59990247-59990263 chr12:59990812-59990825
24	BRCA1	chr12:59988732-59988981	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr12:59842558-59842653	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr12:59940309-59940328	GM12878	blood:	n/a	n/a
27	BRCA1	chr12:59990326-59991667	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr12:59855963-59855973	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr12:59771063-59771145	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr12:59776889-59777702	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr12:59688446-59688498	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr12:59989213-59989930	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr12:59990143-59990337	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr12:59769331-59769379	GM12878	blood:	n/a	n/a
35	BRCA1	chr12:59990664-59990725	GM12878	blood:	n/a	n/a
36	BRCA1	chr12:59964033-59964223	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr12:59990365-59990437	GM12878	blood:	n/a	n/a
38	CEBPB	chr12:59833740-59833840	IMR90	lung:	n/a	n/a
39	CEBPB	chr12:59769408-59769782	ECC-1	luminal epithelium:	n/a	chr12:59769607-59769618
40	CEBPB	chr12:59846095-59846499	IMR90	lung:	n/a	chr12:59846293-59846306 chr12:59846293-59846304
41	CEBPB	chr12:59769435-59769763	K562	blood:	n/a	chr12:59769607-59769618
42	CEBPB	chr12:59847192-59847470	IMR90	lung:	n/a	chr12:59847298-59847311 chr12:59847298-59847311 chr12:59847299-59847310
43	CEBPB	chr12:59797012-59797670	Hela-S3	cervix:	n/a	chr12:59797254-59797265 chr12:59797159-59797172 chr12:59797254-59797267 chr12:59797159-59797172
44	CEBPB	chr12:59795805-59796116	IMR90	lung:	n/a	chr12:59795959-59795970 chr12:59795961-59795972 chr12:59795961-59795970
45	CEBPB	chr12:59990609-59991795	IMR90	lung:	n/a	chr12:59991450-59991461 chr12:59991297-59991309
46	CEBPB	chr12:59795829-59796135	A549	lung:	n/a	chr12:59795959-59795970 chr12:59795961-59795972 chr12:59795961-59795970
47	CEBPB	chr12:59769442-59769765	IMR90	lung:	n/a	chr12:59769607-59769618
48	CEBPB	chr12:59769473-59769784	MCF-7	breast:	n/a	chr12:59769607-59769618
49	CEBPB	chr12:59988714-59991772	Hela-S3	cervix:	n/a	chr12:59991450-59991461 chr12:59988794-59988811 chr12:59988905-59988916 chr12:59991297-59991309 chr12:59988904-59988915
50	CEBPB	chr12:59822731-59822996	HepG2	liver:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:59715992-59716042	AG04450	lung:	fetal
2	chr12:59986233-59986283	H1-hESC	embryonic stem cell:	embryo
3	chr12:59715992-59716042	AG04450	lung:	fetal
4	chr12:59986233-59986283	H1-hESC	embryonic stem cell:	embryo
5	chr12:59925037-59925087	HUVEC	blood vessel:	n/a
6	chr12:59924853-59924903	HNPCEpiC	eye:	n/a
7	chr12:59797287-59797337	U87	brain:	n/a
8	chr12:59990120-59990170	PANC-1	pancreas:	n/a
9	chr12:59990420-59990470	BJ	skin:	n/a
10	chr12:59925323-59925373	AG09319	gingival:	n/a
11	chr12:59990120-59990170	GM12892	blood:	n/a
12	chr12:59989535-59989585	NB4	blood:	n/a
13	chr12:59990794-59990844	LNCaP	prostate:	n/a
14	chr12:59845805-59845855	PANC-1	pancreas:	n/a
15	chr12:59721694-59721744	SK-N-SH_RA	brain:	n/a
16	chr12:59730539-59730589	Hepatocyte	liver:	n/a
17	chr12:59990894-59990944	GM19239	blood:	n/a
18	chr12:59990894-59990944	PFSK-1	brain:	n/a
19	chr12:59990794-59990844	HPAEpiC	pulmonary alveolar:	n/a
20	chr12:59986233-59986283	ProgFib	skin:	n/a
21	chr12:59990794-59990844	Caco-2	colon:	n/a
22	chr12:59989535-59989585	SKMC	muscle:	n/a
23	chr12:59990894-59990944	NT2-D1	testis:	n/a
24	chr12:59730539-59730589	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:59925037-59925087	ovcar-3	ovarian:	n/a
26	chr12:59989742-59989792	SK-N-MC	brain:	n/a
27	chr12:59989535-59989585	SK-N-SH_RA	brain:	n/a
28	chr12:59715992-59716042	NHDF-neo	bronchial:	n/a
29	chr12:59990675-59990725	CMK	blood:	n/a
30	chr12:59721694-59721744	MCF-7	breast:	n/a
31	chr12:59845805-59845855	AG04449	skin:	fetal
32	chr12:59990120-59990170	HCT-116	colon:	n/a
33	chr12:59986233-59986283	HEK293	kidney:	embryo
34	chr12:59990894-59990944	NHDF-neo	bronchial:	n/a
35	chr12:59989652-59989702	GM12878	blood:	n/a
36	chr12:59715992-59716042	HRCEpiC	kidney:	n/a
37	chr12:59989735-59989785	HNPCEpiC	eye:	n/a
38	chr12:59990420-59990470	AG04449	skin:	fetal
39	chr12:59797287-59797337	AoSMC	blood vessel:	n/a
40	chr12:59990794-59990844	PFSK-1	brain:	n/a
41	chr12:59993762-59993812	NHDF-neo	bronchial:	n/a
42	chr12:59993762-59993812	SAEC	small airway:	n/a
43	chr12:59989535-59989585	NHDF-neo	bronchial:	n/a
44	chr12:59845805-59845855	HCT-116	colon:	n/a
45	chr12:59990794-59990844	ProgFib	skin:	n/a
46	chr12:59989535-59989585	SAEC	small airway:	n/a
47	chr12:59990420-59990470	HL-60	blood:	n/a
48	chr12:59845805-59845855	SKMC	muscle:	n/a
49	chr12:59986233-59986283	AoSMC	blood vessel:	n/a
50	chr12:59845805-59845855	K562	blood:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:59828775..59830470-chr12:59832141..59834359,2	K562	blood:
2	chr12:59894898..59897398-chr12:59898807..59901162,2	MCF-7	breast:
3	chr12:59982239..59984090-chr12:59987123..59989672,2	MCF-7	breast:
4	chr12:59975029..59977072-chr12:59989828..59992330,2	MCF-7	breast:
5	chr12:59824786..59825486-chr12:60174654..60175192,2	MCF-7	breast:
6	chr12:59952670..59955367-chr12:59988706..59991381,2	MCF-7	breast:
7	chr12:59990404..59991079-chr15:65596908..65597443,2	Hela-S3	cervix:
8	chr12:59989688..59990375-chr9:133568932..133569541,2	Hela-S3	cervix:
9	chr12:59989792..59990315-chr20:388080..388989,2	Hela-S3	cervix:
10	chr12:59825209..59825865-chr12:60201866..60202550,2	MCF-7	breast:
11	chr12:59692138..59694777-chr12:59713415..59715358,2	MCF-7	breast:
12	chr12:59567506..59568224-chr12:59739584..59740478,2	MCF-7	breast:
13	chr12:59507234..59507853-chr12:59766386..59767199,2	MCF-7	breast:
14	chr12:59998248..60000809-chr12:60000863..60003196,2	MCF-7	breast:
15	chr12:59692138..59694777-chr12:59713415..59715358,2	MCF-7	breast:
16	chr12:59993759..59996018-chr12:59997154..59999022,2	MCF-7	breast:
17	chr12:59819624..59822247-chr12:59822871..59826193,3	K562	blood:
18	chr12:59914091..59917711-chr12:59989940..59992108,3	MCF-7	breast:
19	chr12:59990114..59991690-chr12:59995288..59997168,2	MCF-7	breast:
20	chr12:59983299..59985643-chr12:59988143..59990985,2	K562	blood:
21	chr12:59764978..59768337-chr12:59768399..59771459,3	MCF-7	breast:
22	chr12:59839463..59841278-chr12:59990128..59991816,2	MCF-7	breast:
23	chr12:59982239..59984090-chr12:59987123..59989672,2	MCF-7	breast:
24	chr12:59990837..59991400-chr3:15373811..15374535,2	Hela-S3	cervix:
25	chr12:59989176..59992374-chr12:59998507..60002701,5	MCF-7	breast:
26	chr12:59919709..59922642-chr12:59929595..59932355,2	MCF-7	breast:
27	chr12:59894898..59897398-chr12:59898807..59901162,2	MCF-7	breast:
28	chr12:59987463..59989577-chr12:59995845..59998372,2	MCF-7	breast:
29	chr12:59774582..59777442-chr12:59779741..59781913,2	K562	blood:
30	chr12:59993759..59996018-chr12:59997154..59999022,2	MCF-7	breast:
31	chr12:59971852..59974458-chr12:59976110..59977979,2	K562	blood:
32	chr12:59987463..59989577-chr12:59995845..59998372,2	MCF-7	breast:
33	chr12:59828775..59830470-chr12:59832141..59834359,2	K562	blood:
34	chr12:59990711..59992487-chr12:59993395..59995122,2	MCF-7	breast:
35	chr12:59971852..59974458-chr12:59976110..59977979,2	K562	blood:
36	chr12:59941726..59943985-chr12:59989663..59991635,2	MCF-7	breast:
37	chr12:59567188..59568180-chr12:59766489..59767406,3	MCF-7	breast:
38	chr12:59507468..59508144-chr12:59801341..59801884,3	MCF-7	breast:
39	chr12:59774582..59777442-chr12:59779741..59781913,2	K562	blood:
40	chr12:59819624..59822247-chr12:59822871..59826193,3	K562	blood:
41	chr12:59796807..59797458-chr12:60228606..60229339,3	MCF-7	breast:
42	chr12:59764978..59768337-chr12:59768399..59771459,3	MCF-7	breast:
43	chr12:59838603..59839620-chr12:60174016..60175145,3	MCF-7	breast:
44	chr12:59846048..59848605-chr12:59989591..59991500,2	MCF-7	breast:
45	chr12:59970227..59972157-chr12:59989473..59991716,2	MCF-7	breast:
46	chr12:59507585..59508107-chr12:59766521..59767200,2	MCF-7	breast:
47	chr12:59990876..59991528-chr9:32552220..32553126,2	Hela-S3	cervix:
48	chr12:59802183..59802836-chr20:52395505..52396391,2	MCF-7	breast:
49	chr12:59993257..59995934-chr12:60002294..60005261,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-272B17.2.1-1	chr12:59796972-59797091	ENSG00000258214
2	lnc-SLC16A7-1	chr12:59833557-59835248	XLOC_009783
3	lnc-RP11-272B17.2.1-1	chr12:59804912-59804952	ENSG00000258214
4	lnc-SLC16A7-4	chr12:59712962-59714552	NONHSAT029042
5	lnc-SLC16A7-1	chr12:59832093-59832126	XLOC_009783
6	lnc-SLC16A7-4	chr12:59714688-59717255	NONHSAT029042
7	lnc-RP11-272B17.2.1-1	chr12:59796410-59796544	ENSG00000258214
8	lnc-RP11-272B17.2.1-1	chr12:59759999-59760050	ENSG00000258214

No data

Variant related genes	Relation type
ENSG00000258214	TF binding region
RNU6-871P	TF binding region
RNU6-279P	TF binding region
ENSG00000266724	TF binding region
ENSG00000257230	TF binding region
RNU4-20P	TF binding region
ENSG00000265430	TF binding region
SLC16A7	TF binding region
ENSG00000258214	CpG island
RNU6-871P	CpG island
RNU6-279P	CpG island
ENSG00000266724	CpG island
ENSG00000257230	CpG island
RNU4-20P	CpG island
ENSG00000265430	CpG island
SLC16A7	CpG island
ENSG00000197579	chromatin interactions
ENSG00000266724	chromatin interactions
ENSG00000235453	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000125826	chromatin interactions
ENSG00000130713	chromatin interactions
ENSG00000131370	chromatin interactions
ENSG00000118596	chromatin interactions
ENSG00000265430	chromatin interactions
KIF1B	miRNA target sites

Extended variants
information (count: 8025 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:8025 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192248071	chr12:59683615-59683616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541339984	chr12:59683617-59683618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547058611	chr12:59683679-59683680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371994216	chr12:59683709-59683710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558935916	chr12:59683722-59683723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529689120	chr12:59683789-59683790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1500030	chr12:59683869-59683870	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs371209279	chr12:59683921-59683922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567907480	chr12:59683926-59683927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538494066	chr12:59683927-59683928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574924969	chr12:59684053-59684054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543999142	chr12:59684074-59684075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562527837	chr12:59684080-59684081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571841300	chr12:59684087-59684088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539151947	chr12:59684139-59684140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556862561	chr12:59684168-59684169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554342547	chr12:59684229-59684230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531451651	chr12:59684233-59684234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184635367	chr12:59684249-59684250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551369345	chr12:59684271-59684272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554937989	chr12:59684311-59684312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568046664	chr12:59684312-59684313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564854699	chr12:59684338-59684339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576266949	chr12:59684339-59684340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576655035	chr12:59684381-59684382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527317891	chr12:59684420-59684421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189194178	chr12:59684462-59684463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368295619	chr12:59684465-59684466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113036561	chr12:59684489-59684490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376145766	chr12:59684585-59684586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540809738	chr12:59684589-59684590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7314308	chr12:59684714-59684715	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs76194613	chr12:59684729-59684730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547888057	chr12:59684734-59684735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563252007	chr12:59684745-59684746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549571369	chr12:59684768-59684769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181059881	chr12:59684882-59684883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550462388	chr12:59684949-59684950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184058596	chr12:59685013-59685014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539264950	chr12:59685014-59685015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145780091	chr12:59685024-59685025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548008232	chr12:59685034-59685035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs117443039	chr12:59685037-59685038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188839128	chr12:59685043-59685044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11172988	chr12:59685045-59685046	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs149188697	chr12:59685048-59685049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558653283	chr12:59685055-59685056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs367949354	chr12:59685061-59685062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201766474	chr12:59685078-59685079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs66734435	chr12:59685079-59685080	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1421 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59683600-59688000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:59684000-59684200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:59684200-59684800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr12:59684800-59685600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr12:59686400-59687000	Enhancers	Gastric	stomach
6	chr12:59687000-59687200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr12:59687000-59692200	Weak transcription	Gastric	stomach
8	chr12:59688000-59688200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:59688200-59688600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:59688600-59689000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:59690200-59690400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr12:59690400-59692200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr12:59692200-59692400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr12:59692200-59692400	Enhancers	Gastric	stomach
15	chr12:59697400-59698600	Enhancers	Fetal Heart	heart
16	chr12:59698200-59698400	Enhancers	Aorta	Aorta
17	chr12:59704600-59707400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr12:59705400-59707400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:59707200-59709000	Enhancers	Brain Germinal Matrix	brain
20	chr12:59707400-59707600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:59707400-59713400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr12:59707600-59708000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:59708000-59708200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:59708200-59714000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:59709800-59710000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
26	chr12:59710000-59710800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr12:59710800-59711200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr12:59711200-59711400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr12:59711200-59711600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr12:59711200-59711800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr12:59711400-59711600	Enhancers	H9 Cell Line	embryonic stem cell
32	chr12:59711400-59711600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr12:59711400-59712000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr12:59711400-59714400	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr12:59711400-59715000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr12:59711600-59712800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr12:59711600-59715000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr12:59711600-59715200	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr12:59711800-59712000	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr12:59711800-59713400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr12:59711800-59716200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr12:59712000-59714200	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr12:59712000-59715000	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr12:59712800-59714200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
45	chr12:59713400-59713600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr12:59713400-59715200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:59713400-59716000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
48	chr12:59713600-59715200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr12:59714000-59714200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr12:59714000-59715200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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