Variant report

Variant	nsv946387
Chromosome Location	chr1:151521876-151530261
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:151526221-151526491	GM12878	blood:	n/a	chr1:151526316-151526327
2	CEBPB	chr1:151529142-151529689	A549	lung:	n/a	chr1:151529400-151529411
3	CEBPB	chr1:151526081-151526425	IMR90	lung:	n/a	n/a
4	CEBPB	chr1:151529259-151529634	A549	lung:	n/a	chr1:151529400-151529411
5	CEBPB	chr1:151521086-151522302	A549	lung:	n/a	n/a
6	CEBPB	chr1:151529253-151529526	HepG2	liver:	n/a	chr1:151529400-151529411
7	CEBPB	chr1:151529295-151529513	H1-hESC	embryonic stem cell:	n/a	chr1:151529400-151529411
8	CEBPB	chr1:151529150-151529594	MCF-7	breast:	n/a	chr1:151529400-151529411
9	CEBPB	chr1:151529262-151529518	Hela-S3	cervix:	n/a	chr1:151529400-151529411
10	CEBPB	chr1:151529200-151529535	K562	blood:	n/a	chr1:151529400-151529411
11	CEBPB	chr1:151529254-151529515	K562	blood:	n/a	chr1:151529400-151529411
12	CEBPB	chr1:151529252-151529506	IMR90	lung:	n/a	chr1:151529400-151529411
13	CEBPB	chr1:151529263-151529501	A549	lung:	n/a	chr1:151529400-151529411
14	CEBPB	chr1:151522072-151522141	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:151529141-151529677	MCF-7	breast:	n/a	chr1:151529400-151529411
16	CEBPB	chr1:151529304-151529439	HepG2	liver:	n/a	chr1:151529400-151529411
17	CTCF	chr1:151521760-151521910	MCF-7	breast:	n/a	n/a
18	CTCF	chr1:151521900-151522050	Caco-2	colon:	n/a	n/a
19	CTCF	chr1:151521860-151522010	AG10803	skin:	n/a	n/a
20	CTCF	chr1:151527100-151527250	K562	blood:	n/a	n/a
21	EGR1	chr1:151525646-151525899	K562	blood:	n/a	n/a
22	EGR1	chr1:151525731-151525904	K562	blood:	n/a	n/a
23	ELF1	chr1:151520997-151521910	MCF-7	breast:	n/a	n/a
24	EP300	chr1:151521056-151521906	A549	lung:	n/a	chr1:151521257-151521266
25	EP300	chr1:151521036-151522306	A549	lung:	n/a	chr1:151521257-151521266
26	EP300	chr1:151526753-151526764	K562	blood:	n/a	n/a
27	FOS	chr1:151526269-151526390	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr1:151526309-151526470	MCF10A-Er-Src	breast:	n/a	n/a
29	FOSL2	chr1:151521055-151521887	MCF-7	breast:	n/a	chr1:151521497-151521509 chr1:151521856-151521866 chr1:151521314-151521328 chr1:151521856-151521866 chr1:151521496-151521507 chr1:151521499-151521507
30	FOSL2	chr1:151521055-151522095	A549	lung:	n/a	chr1:151521497-151521509 chr1:151521856-151521866 chr1:151521314-151521328 chr1:151521856-151521866 chr1:151521496-151521507 chr1:151521499-151521507
31	FOXA2	chr1:151521239-151521957	A549	lung:	n/a	n/a
32	GABPA	chr1:151521034-151521903	MCF-7	breast:	n/a	n/a
33	GATA3	chr1:151526110-151526746	SK-N-SH	brain:	n/a	n/a
34	GATA3	chr1:151526061-151526525	SK-N-SH	brain:	n/a	n/a
35	GATA3	chr1:151520900-151522119	A549	lung:	n/a	chr1:151521497-151521506 chr1:151521428-151521437 chr1:151521427-151521437 chr1:151521427-151521435 chr1:151521428-151521435
36	GATA3	chr1:151521077-151521940	SK-N-SH	brain:	n/a	chr1:151521497-151521506 chr1:151521428-151521437 chr1:151521427-151521437 chr1:151521427-151521435 chr1:151521428-151521435
37	GATA3	chr1:151520890-151521893	MCF-7	breast:	n/a	chr1:151521497-151521506 chr1:151521428-151521437 chr1:151521427-151521437 chr1:151521427-151521435 chr1:151521428-151521435
38	GATA3	chr1:151519199-151522048	MCF-7	breast:	n/a	chr1:151521497-151521506 chr1:151521428-151521437 chr1:151521427-151521437 chr1:151521427-151521435 chr1:151521428-151521435 chr1:151520014-151520024
39	HDAC2	chr1:151521203-151522034	MCF-7	breast:	n/a	chr1:151521427-151521436
40	HDAC2	chr1:151521043-151522064	MCF-7	breast:	n/a	chr1:151521427-151521436
41	JUND	chr1:151521154-151522022	SK-N-SH	brain:	n/a	chr1:151521497-151521509 chr1:151521856-151521866 chr1:151521314-151521328 chr1:151521856-151521866 chr1:151521499-151521507 chr1:151521497-151521508
42	JUND	chr1:151520976-151521933	MCF-7	breast:	n/a	chr1:151521497-151521509 chr1:151521856-151521866 chr1:151521314-151521328 chr1:151521856-151521866 chr1:151521499-151521507 chr1:151521497-151521508
43	JUND	chr1:151521180-151521972	A549	lung:	n/a	chr1:151521497-151521509 chr1:151521856-151521866 chr1:151521314-151521328 chr1:151521856-151521866 chr1:151521499-151521507 chr1:151521497-151521508
44	KAP1	chr1:151521268-151522256	HEK293	kidney:	n/a	n/a
45	MAFK	chr1:151521199-151521965	Hela-S3	cervix:	n/a	n/a
46	MAX	chr1:151520976-151522105	A549	lung:	n/a	chr1:151521915-151521924 chr1:151521479-151521489
47	MAX	chr1:151521017-151522242	MCF-7	breast:	n/a	chr1:151521915-151521924 chr1:151521479-151521489
48	NFIC	chr1:151526096-151526587	SK-N-SH	brain:	n/a	n/a
49	NR2F2	chr1:151520972-151522506	MCF-7	breast:	n/a	n/a
50	NR2F2	chr1:151521018-151522005	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:151525489..151528201-chr1:151689463..151691011,2	MCF-7	breast:
2	1:151516085-151535167..1:151592347-151603110	GM12878	blood:
3	chr1:151518630..151520620-chr1:151521717..151523479,2	K562	blood:
4	chr1:151512668..151514795-chr1:151529335..151532212,2	K562	blood:
5	chr1:151520214..151522047-chr1:151540698..151542766,2	MCF-7	breast:
6	chr1:151511607..151517154-chr1:151519761..151524773,6	K562	blood:
7	chr1:151520240..151522190-chr1:151976261..151978118,2	MCF-7	breast:
8	chr1:151520439..151521960-chr1:151523867..151525775,2	K562	blood:
9	chr1:151522558..151525413-chr1:151540386..151543231,3	MCF-7	breast:
10	chr1:151526189..151529044-chr1:151534170..151536769,2	MCF-7	breast:
11	1:151171193-151178589..1:151516085-151535167	GM12878	blood:
12	chr1:151489014..151491832-chr1:151520153..151522189,2	MCF-7	breast:
13	chr1:151528431..151531724-chr1:151533235..151535890,3	K562	blood:
14	chr1:151481542..151488437-chr1:151515636..151525415,14	MCF-7	breast:
15	chr1:151526616..151529320-chr1:151540801..151542682,2	MCF-7	breast:
16	chr1:151519770..151522144-chr1:151805041..151806645,2	MCF-7	breast:
17	chr1:151429392..151432679-chr1:151519688..151523512,7	MCF-7	breast:
18	1:151402394-151411623..1:151516085-151535167	GM12878	blood:
19	chr1:151519173..151521651-chr1:151523857..151526108,3	MCF-7	breast:
20	chr1:151511080..151515753-chr1:151520278..151524135,5	K562	blood:
21	chr1:151430069..151432862-chr1:151521024..151523772,3	MCF-7	breast:
22	chr1:151483462..151487382-chr1:151518217..151524477,9	MCF-7	breast:
23	chr1:151518255..151520470-chr1:151528849..151531247,2	MCF-7	breast:
24	chr1:151528421..151530199-chr1:151537173..151538889,2	K562	blood:
25	chr1:151511342..151513361-chr1:151529767..151532080,2	MCF-7	breast:
26	chr1:151524039..151526579-chr1:151544817..151547592,2	MCF-7	breast:
27	chr1:151528431..151530399-chr1:151533235..151535890,2	K562	blood:
28	chr1:151521243..151523958-chr1:151534794..151537419,2	MCF-7	breast:
29	chr1:151520439..151521960-chr1:151523867..151525775,2	K562	blood:

Variant related genes	Relation type
ENSG00000223861	TF binding region
TUFT1	TF binding region
ENSG00000143442	chromatin interactions
ENSG00000143398	chromatin interactions
ENSG00000238711	chromatin interactions
ENSG00000207606	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000206635	chromatin interactions
ENSG00000143375	chromatin interactions

Extended variants
information (count: 296 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17640579	chr1:151521933-151521934	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536090573	chr1:151521941-151521942	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs555975701	chr1:151521995-151521996	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs575460145	chr1:151522018-151522019	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs137877570	chr1:151522038-151522039	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs557480321	chr1:151522077-151522078	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs558786402	chr1:151522079-151522080	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs6672827	chr1:151522080-151522081	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs577128431	chr1:151522140-151522141	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs144113865	chr1:151522171-151522172	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs544297534	chr1:151522207-151522208	Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs371782496	chr1:151522222-151522223	Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs6673041	chr1:151522278-151522279	Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs573573669	chr1:151522307-151522308	Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs116192488	chr1:151522309-151522310	Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs192673300	chr1:151522318-151522319	Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs147335302	chr1:151522322-151522323	Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs544646139	chr1:151522373-151522374	Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs141001047	chr1:151522376-151522377	Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs377264544	chr1:151522389-151522390	Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs529974795	chr1:151522409-151522410	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs533325569	chr1:151522433-151522434	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs372139442	chr1:151522477-151522478	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs546663300	chr1:151522491-151522492	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs567200136	chr1:151522507-151522508	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs374781009	chr1:151522523-151522524	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs529610091	chr1:151522611-151522612	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs549641766	chr1:151522612-151522613	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs569437195	chr1:151522614-151522615	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs537549016	chr1:151522630-151522631	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs146310619	chr1:151522673-151522674	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs377255639	chr1:151522675-151522676	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs557808930	chr1:151522697-151522698	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs542032081	chr1:151522788-151522789	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs544051443	chr1:151522803-151522804	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs571237155	chr1:151522821-151522822	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs373168620	chr1:151522823-151522824	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs144782292	chr1:151522863-151522864	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs369436004	chr1:151522870-151522871	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs184334019	chr1:151522877-151522878	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs573636331	chr1:151522881-151522882	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs148537214	chr1:151522882-151522883	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs373351738	chr1:151522945-151522946	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs555942280	chr1:151523043-151523044	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs576157645	chr1:151523073-151523074	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs142847870	chr1:151523087-151523088	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs151041538	chr1:151523103-151523104	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs188191331	chr1:151523254-151523255	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs540670680	chr1:151523279-151523280	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs560431675	chr1:151523305-151523306	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151514400-151540800	Weak transcription	Brain Angular Gyrus	brain
2	chr1:151514400-151556800	Weak transcription	Fetal Brain Male	brain
3	chr1:151515400-151523400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:151515600-151534400	Weak transcription	Brain Germinal Matrix	brain
5	chr1:151517400-151522200	Enhancers	Placenta Amnion	Placenta Amnion
6	chr1:151517600-151523400	Enhancers	Placenta	Placenta
7	chr1:151518200-151522200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:151518400-151522800	Enhancers	Fetal Intestine Large	intestine
9	chr1:151518600-151522000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:151519200-151522200	Flanking Active TSS	A549	lung
11	chr1:151519400-151522000	Enhancers	Duodenum Mucosa	Duodenum
12	chr1:151519400-151522000	Enhancers	Pancreas	Pancrea
13	chr1:151519400-151522000	Enhancers	HUVEC	blood vessel
14	chr1:151519400-151522200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:151519400-151522200	Flanking Active TSS	Hela-S3	cervix
16	chr1:151519400-151522400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr1:151519400-151522400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:151519400-151522400	Enhancers	Stomach Mucosa	stomach
19	chr1:151519400-151522600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:151519400-151522800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:151519600-151522000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr1:151519600-151522400	Enhancers	Gastric	stomach
23	chr1:151519600-151522400	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr1:151519600-151524400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr1:151519800-151522000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:151520000-151522000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr1:151520000-151522000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:151520200-151522000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr1:151520200-151522200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr1:151520200-151524000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr1:151520200-151524600	Weak transcription	Right Atrium	heart
32	chr1:151520200-151534200	Weak transcription	Fetal Stomach	stomach
33	chr1:151520200-151536600	Weak transcription	Ovary	ovary
34	chr1:151520400-151522000	Enhancers	NHDF-Ad	bronchial
35	chr1:151520400-151522200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr1:151520400-151522200	Enhancers	HSMM	muscle
37	chr1:151520400-151522200	Enhancers	NH-A	brain
38	chr1:151520400-151522600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:151520400-151522600	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr1:151520400-151534200	Weak transcription	Stomach Smooth Muscle	stomach
41	chr1:151520400-151535800	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr1:151520400-151536600	Weak transcription	Adipose Nuclei	Adipose
43	chr1:151520400-151536800	Weak transcription	Aorta	Aorta
44	chr1:151520600-151522200	Enhancers	NHLF	lung
45	chr1:151520600-151522600	Enhancers	HMEC	breast
46	chr1:151520600-151522800	Enhancers	HepG2	liver
47	chr1:151520600-151536000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr1:151520600-151536800	Weak transcription	Lung	lung
49	chr1:151520600-151542000	Weak transcription	Right Ventricle	heart
50	chr1:151520600-151545200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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