Variant report

Variant	nsv872544
Chromosome Location	chr1:171616822-171654968
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	ARID3A	chr1:171626520-171626562	K562	blood:	n/a	n/a
2	ARID3A	chr1:171622941-171623297	HepG2	liver:	n/a	n/a
3	ATF1	chr1:171653118-171653351	K562	blood:	n/a	n/a
4	BACH1	chr1:171624806-171624860	K562	blood:	n/a	n/a
5	BACH1	chr1:171637655-171637698	K562	blood:	n/a	n/a
6	BHLHE40	chr1:171624657-171624962	K562	blood:	n/a	n/a
7	BHLHE40	chr1:171625476-171625683	HepG2	liver:	n/a	n/a
8	CBX3	chr1:171624606-171625002	K562	blood:	n/a	n/a
9	CEBPB	chr1:171650931-171651210	K562	blood:	n/a	chr1:171651025-171651036
10	CEBPB	chr1:171650920-171651113	A549	lung:	n/a	chr1:171651025-171651036
11	CEBPB	chr1:171650860-171651190	HepG2	liver:	n/a	chr1:171651025-171651036
12	CHD2	chr1:171624679-171625014	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr1:171624466-171624580	GM12891	blood:	n/a	n/a
14	CTCF	chr1:171624780-171624930	GM12864	blood:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
15	CTCF	chr1:171624720-171624870	HCT-116	colon:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
16	CTCF	chr1:171624760-171624910	AG09319	gingival:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
17	CTCF	chr1:171624820-171624970	RPTEC	kidney:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
18	CTCF	chr1:171624693-171624900	Lung_OC	lung:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
19	CTCF	chr1:171624686-171624955	GM13977	blood:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
20	CTCF	chr1:171624780-171624930	HVMF	connective:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
21	CTCF	chr1:171624300-171624450	GM12864	blood:	n/a	n/a
22	CTCF	chr1:171624740-171624890	HVMF	connective:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
23	CTCF	chr1:171624700-171624850	HEEpiC	esophagus:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
24	CTCF	chr1:171624420-171624570	GM12872	blood:	n/a	n/a
25	CTCF	chr1:171624565-171624990	K562	blood:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
26	CTCF	chr1:171625220-171625370	GM12871	blood:	n/a	n/a
27	CTCF	chr1:171624760-171624910	HRPEpiC	eye:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
28	CTCF	chr1:171624489-171624561	GM12878	blood:	n/a	n/a
29	CTCF	chr1:171624740-171624890	NHDF-neo	bronchial:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
30	CTCF	chr1:171624744-171624891	Pancreas_OC	pancreas:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
31	CTCF	chr1:171624668-171624966	GM19240	blood:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
32	CTCF	chr1:171624647-171624925	SK-N-SH_RA	brain:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
33	CTCF	chr1:171624760-171624910	A549	lung:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
34	CTCF	chr1:171624760-171624910	HBMEC	blood vessel:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
35	CTCF	chr1:171624572-171625001	H1-hESC	embryonic stem cell:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
36	CTCF	chr1:171624740-171624890	Caco-2	colon:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
37	CTCF	chr1:171624700-171624850	HFF-Myc	foreskin:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
38	CTCF	chr1:171624645-171624997	A549	lung:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
39	CTCF	chr1:171624645-171624967	GM12891	blood:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
40	CTCF	chr1:171624678-171624989	GM12878	blood:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
41	CTCF	chr1:171624800-171624950	WI-38	lung:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
42	CTCF	chr1:171624645-171625001	IMR90	lung:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
43	CTCF	chr1:171624740-171624890	GM12868	blood:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
44	CTCF	chr1:171624020-171624170	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr1:171624479-171625176	SK-N-SH	brain:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
46	CTCF	chr1:171624780-171624930	HRPEpiC	eye:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
47	CTCF	chr1:171639658-171639817	T-47D	breast:	n/a	n/a
48	CTCF	chr1:171624663-171624949	H1-hESC	embryonic stem cell:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
49	CTCF	chr1:171624720-171624870	HUVEC	blood vessel:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836
50	CTCF	chr1:171624720-171624870	HPF	lung:	n/a	chr1:171624822-171624838 chr1:171624824-171624837 chr1:171624821-171624839 chr1:171624826-171624836

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:171623695-171623745	HRPEpiC	eye:	n/a
2	chr1:171636428-171636478	RPTEC	kidney:	n/a
3	chr1:171623695-171623745	HRPEpiC	eye:	n/a
4	chr1:171636428-171636478	RPTEC	kidney:	n/a
5	chr1:171622329-171622379	SAEC	small airway:	n/a
6	chr1:171640387-171640437	HCT-116	colon:	n/a
7	chr1:171623695-171623745	HCM	heart:	n/a
8	chr1:171622329-171622379	HCPEpiC	choroid plexus:	n/a
9	chr1:171640211-171640261	NB4	blood:	n/a
10	chr1:171639856-171639906	HL-60	blood:	n/a
11	chr1:171640211-171640261	HUVEC	blood vessel:	n/a
12	chr1:171636428-171636478	HRE	kidney:	n/a
13	chr1:171621834-171621884	PANC-1	pancreas:	n/a
14	chr1:171623695-171623745	ECC-1	luminal epithelium:	n/a
15	chr1:171640223-171640273	GM12878	blood:	n/a
16	chr1:171621834-171621884	LNCaP	prostate:	n/a
17	chr1:171640223-171640273	IMR90	lung:	fetal
18	chr1:171640211-171640261	NHDF-neo	bronchial:	n/a
19	chr1:171636428-171636478	BE2_C	brain:	n/a
20	chr1:171640223-171640273	T-47D	breast:	n/a
21	chr1:171623695-171623745	HCPEpiC	choroid plexus:	n/a
22	chr1:171639856-171639906	K562	blood:	n/a
23	chr1:171621279-171621329	HRPEpiC	eye:	n/a
24	chr1:171640223-171640273	ProgFib	skin:	n/a
25	chr1:171621941-171621991	SK-N-SH_RA	brain:	n/a
26	chr1:171621834-171621884	NHBE	bronchial:	n/a
27	chr1:171640211-171640261	AG10803	skin:	n/a
28	chr1:171640102-171640152	HRCEpiC	kidney:	n/a
29	chr1:171621941-171621991	HUVEC	blood vessel:	n/a
30	chr1:171640211-171640261	SK-N-MC	brain:	n/a
31	chr1:171621941-171621991	LNCaP	prostate:	n/a
32	chr1:171640223-171640273	NHBE	bronchial:	n/a
33	chr1:171623695-171623745	SKMC	muscle:	n/a
34	chr1:171621834-171621884	HAEpiC	amniotic membrane:	n/a
35	chr1:171636428-171636478	SAEC	small airway:	n/a
36	chr1:171621834-171621884	Jurkat	blood:	n/a
37	chr1:171640223-171640273	GM19239	blood:	n/a
38	chr1:171636428-171636478	AG04449	skin:	fetal
39	chr1:171640102-171640152	PANC-1	pancreas:	n/a
40	chr1:171621732-171621782	MCF-7	breast:	n/a
41	chr1:171623695-171623745	T-47D	breast:	n/a
42	chr1:171621279-171621329	NHDF-neo	bronchial:	n/a
43	chr1:171622329-171622379	HCF	heart:	n/a
44	chr1:171621941-171621991	HCPEpiC	choroid plexus:	n/a
45	chr1:171640387-171640437	AG04449	skin:	fetal
46	chr1:171623695-171623745	GM12891	blood:	n/a
47	chr1:171621732-171621782	GM12891	blood:	n/a
48	chr1:171621941-171621991	A549	lung:	n/a
49	chr1:171621732-171621782	LNCaP	prostate:	n/a
50	chr1:171640102-171640152	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:171640488..171642353-chr1:171643288..171645992,2	K562	blood:
2	chr1:171624400..171625332-chr1:171684735..171685281,3	K562	blood:
3	chr1:171614371..171616986-chr1:171628195..171631368,3	K562	blood:
4	chr1:171624257..171625200-chr1:171684733..171685343,5	MCF-7	breast:
5	chr1:171625427..171627489-chr1:171632106..171634164,2	K562	blood:
6	chr1:171624474..171625267-chr1:171684716..171685707,4	MCF-7	breast:
7	chr1:171624621..171625330-chr1:171953992..171954655,2	K562	blood:
8	chr1:171625427..171627489-chr1:171632106..171634164,2	K562	blood:
9	chr1:171613993..171614607-chr1:171624519..171625315,2	MCF-7	breast:
10	chr1:171624340..171624863-chr1:171952455..171953150,2	K562	blood:
11	chr1:171635591..171636506-chrX:104332383..104332975,2	MCF-7	breast:
12	chr1:171623874..171626323-chr1:171708681..171711250,2	K562	blood:
13	chr1:171634616..171637711-chr1:171639891..171642261,3	K562	blood:
14	chr1:171642202..171644426-chr1:171645702..171648061,2	K562	blood:
15	chr1:171642979..171645264-chr1:171671539..171674041,2	MCF-7	breast:
16	chr1:171640488..171642353-chr1:171643288..171645992,2	K562	blood:
17	chr1:171642202..171644426-chr1:171645702..171648061,2	K562	blood:
18	chr1:171635500..171638111-chr3:64007265..64009598,2	MCF-7	breast:
19	chr1:171614371..171616986-chr1:171628195..171631368,3	K562	blood:
20	chr1:171618444..171621917-chr1:171624017..171626963,3	K562	blood:
21	chr1:171453576..171455462-chr1:171624270..171626340,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VAMP4-4	chr1:171653921-171654384	l_147_chr1:171653920-171677715_76bGuttman_hLF
2	lnc-VAMP4-4	chr1:171653836-171654384	NONHSAT007577
3	lnc-VAMP4-4	chr1:171653555-171654384	NONHSAT007576

Variant related genes	Relation type
MYOC	TF binding region
PFN1P1	TF binding region
RPL4P3	TF binding region
MYOC	CpG island
PFN1P1	CpG island
RPL4P3	CpG island
ENSG00000034971	chromatin interactions
ENSG00000233328	chromatin interactions
ENSG00000117533	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000117523	chromatin interactions

Extended variants
information (count: 1489 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1489 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182907	chr1:171616822-171616823	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549018242	chr1:171616877-171616878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560771655	chr1:171616892-171616893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531319207	chr1:171616959-171616960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183847618	chr1:171616971-171616972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372244858	chr1:171616974-171616975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs146049671	chr1:171617040-171617041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568887284	chr1:171617045-171617046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140034894	chr1:171617046-171617047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367943284	chr1:171617055-171617056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565489875	chr1:171617153-171617154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs10913389	chr1:171617189-171617190	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs555822672	chr1:171617195-171617196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189016105	chr1:171617234-171617235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191879785	chr1:171617261-171617262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556569511	chr1:171617287-171617288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185718997	chr1:171617292-171617293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12081180	chr1:171617293-171617294	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs9660235	chr1:171617321-171617322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572675630	chr1:171617323-171617324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11295938	chr1:171617329-171617330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529437887	chr1:171617330-171617331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75866173	chr1:171617344-171617345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533780995	chr1:171617366-171617367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542390494	chr1:171617369-171617370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561014640	chr1:171617374-171617375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs6425363	chr1:171617393-171617394	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs549762904	chr1:171617479-171617480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570525773	chr1:171617490-171617491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116662210	chr1:171617525-171617526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74122903	chr1:171617657-171617658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181071580	chr1:171617700-171617701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6425364	chr1:171617708-171617709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs372206251	chr1:171617737-171617738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116423287	chr1:171617762-171617763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7547721	chr1:171617765-171617766	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs200174025	chr1:171617769-171617770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200786827	chr1:171617771-171617772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12078420	chr1:171617827-171617828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571624968	chr1:171617859-171617860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372913762	chr1:171617888-171617889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539389516	chr1:171617889-171617890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142641252	chr1:171617897-171617898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150985414	chr1:171617910-171617911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543225762	chr1:171617922-171617923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554827111	chr1:171617988-171617989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576094661	chr1:171618052-171618053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543066758	chr1:171618076-171618077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7548037	chr1:171618124-171618125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536572275	chr1:171618133-171618134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171614200-171619000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr1:171614600-171624600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:171615200-171623600	Weak transcription	Right Atrium	heart
4	chr1:171615400-171619000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr1:171615400-171620400	Weak transcription	Fetal Muscle Leg	muscle
6	chr1:171615400-171621000	Weak transcription	Left Ventricle	heart
7	chr1:171615400-171621200	Weak transcription	Aorta	Aorta
8	chr1:171615400-171621600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr1:171615400-171622800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr1:171615400-171623000	Weak transcription	HSMM	muscle
11	chr1:171615600-171620000	Weak transcription	Fetal Heart	heart
12	chr1:171615600-171621600	Weak transcription	Liver	Liver
13	chr1:171616200-171618800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:171616400-171621400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:171616600-171617400	Enhancers	Placenta	Placenta
16	chr1:171619000-171621000	Active TSS	Stomach Smooth Muscle	stomach
17	chr1:171620000-171621600	Active TSS	Adipose Nuclei	Adipose
18	chr1:171620000-171623400	Enhancers	Fetal Heart	heart
19	chr1:171620200-171620600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:171620400-171627600	Enhancers	Fetal Muscle Leg	muscle
21	chr1:171620600-171621000	Weak transcription	Fetal Muscle Trunk	muscle
22	chr1:171620800-171621000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr1:171620800-171621400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:171620800-171622600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:171621000-171621200	Active TSS	Colon Smooth Muscle	Colon
26	chr1:171621000-171621400	Enhancers	Fetal Muscle Trunk	muscle
27	chr1:171621000-171621600	Enhancers	Left Ventricle	heart
28	chr1:171621000-171622400	Flanking Active TSS	Stomach Smooth Muscle	stomach
29	chr1:171621000-171624800	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr1:171621000-171625800	Enhancers	Fetal Stomach	stomach
31	chr1:171621200-171621400	Flanking Active TSS	Colon Smooth Muscle	Colon
32	chr1:171621200-171621800	Enhancers	Aorta	Aorta
33	chr1:171621200-171622400	Enhancers	Psoas Muscle	Psoas
34	chr1:171621400-171621600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr1:171621400-171621800	Enhancers	Lung	lung
36	chr1:171621400-171621800	Enhancers	Ovary	ovary
37	chr1:171621400-171621800	Active TSS	Skeletal Muscle Male	skeletal muscle
38	chr1:171621400-171622000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr1:171621400-171622000	Enhancers	Placenta	Placenta
40	chr1:171621400-171622400	Enhancers	Right Ventricle	heart
41	chr1:171621400-171623400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:171621400-171623600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:171621400-171624200	Enhancers	Colon Smooth Muscle	Colon
44	chr1:171621400-171624600	Enhancers	Rectal Smooth Muscle	rectum
45	chr1:171621600-171621800	Enhancers	Colonic Mucosa	Colon
46	chr1:171621600-171622400	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr1:171621600-171623000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr1:171621600-171623200	Weak transcription	Adipose Nuclei	Adipose
49	chr1:171621600-171623200	Enhancers	Liver	Liver
50	chr1:171621600-171623600	Weak transcription	Left Ventricle	heart

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