Variant report

Variant	nsv872597
Chromosome Location	chr1:186646480-186649485
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	ATF3	chr1:186649301-186649931	A549	lung:	n/a	n/a
2	ATF3	chr1:186649257-186649868	A549	lung:	n/a	n/a
3	BACH1	chr1:186649246-186649635	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr1:186649013-186650057	A549	lung:	n/a	chr1:186650009-186650022 chr1:186650012-186650021 chr1:186650006-186650019 chr1:186649718-186649727 chr1:186650010-186650023 chr1:186650009-186650018 chr1:186649344-186649357
5	BCL3	chr1:186649029-186650035	A549	lung:	n/a	chr1:186650009-186650022 chr1:186650012-186650021 chr1:186650006-186650019 chr1:186649718-186649727 chr1:186650010-186650023 chr1:186650009-186650018 chr1:186649344-186649357
6	BRCA1	chr1:186649014-186649898	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr1:186649095-186649898	HCT-116	colon:	n/a	n/a
8	CEBPB	chr1:186649165-186649952	HCT-116	colon:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
9	CEBPB	chr1:186649209-186649865	H1-hESC	embryonic stem cell:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
10	CEBPB	chr1:186649073-186650354	Hela-S3	cervix:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
11	CEBPB	chr1:186649433-186649949	IMR90	lung:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
12	CEBPB	chr1:186649387-186649938	A549	lung:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
13	CEBPB	chr1:186649254-186650099	A549	lung:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
14	CEBPB	chr1:186649370-186649884	MCF-7	breast:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
15	CEBPB	chr1:186649223-186650014	ECC-1	luminal epithelium:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
16	CEBPB	chr1:186649420-186650142	A549	lung:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
17	CEBPB	chr1:186649446-186649905	ECC-1	luminal epithelium:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
18	CHD2	chr1:186649308-186649674	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr1:186649176-186650578	Hela-S3	cervix:	n/a	n/a
20	CREB1	chr1:186649354-186649914	A549	lung:	n/a	n/a
21	CREB1	chr1:186649137-186649803	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr1:186649218-186649743	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr1:186649244-186649965	A549	lung:	n/a	n/a
24	CREB1	chr1:186649314-186649816	GM12878	blood:	n/a	n/a
25	CTBP2	chr1:186649204-186650086	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr1:186649320-186649608	Pancreas_OC	pancreas:	n/a	n/a
27	CTCF	chr1:186649461-186649519	LNCaP	prostate:	n/a	n/a
28	CTCF	chr1:186649420-186649570	HCM	heart:	n/a	n/a
29	CTCF	chr1:186649205-186649591	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:186649400-186649550	GM12867	blood:	n/a	n/a
31	CTCF	chr1:186649460-186649610	HEK293	kidney:	n/a	n/a
32	CTCF	chr1:186649447-186649532	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr1:186649298-186649614	GM13976	blood:	n/a	n/a
34	CTCF	chr1:186649400-186649550	HVMF	connective:	n/a	n/a
35	CTCF	chr1:186649420-186649570	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr1:186649420-186649570	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr1:186649340-186649490	GM12878	blood:	n/a	n/a
38	CTCF	chr1:186649440-186649590	HFF	foreskin:	n/a	n/a
39	CTCF	chr1:186649420-186649570	HCT-116	colon:	n/a	n/a
40	CTCF	chr1:186649400-186649550	GM12874	blood:	n/a	n/a
41	CTCF	chr1:186649400-186649550	NHEK	skin:	n/a	n/a
42	CTCF	chr1:186649460-186649610	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr1:186649256-186649632	GM19238	blood:	n/a	n/a
44	CTCF	chr1:186649370-186649443	GM20000	blood:	n/a	n/a
45	CTCF	chr1:186649380-186649530	GM12870	blood:	n/a	n/a
46	CTCF	chr1:186649400-186649550	AG04449	skin:	n/a	n/a
47	CTCF	chr1:186649420-186649604	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr1:186649460-186649610	GM06990	blood:	n/a	n/a
49	CTCF	chr1:186649322-186649571	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr1:186649440-186649590	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:186649330-186649380	AG09319	gingival:	n/a
2	chr1:186649253-186649303	GM12878	blood:	n/a
3	chr1:186649354-186649404	NHDF-neo	bronchial:	n/a
4	chr1:186649354-186649404	AG04450	lung:	fetal
5	chr1:186649253-186649303	SK-N-MC	brain:	n/a
6	chr1:186649330-186649380	SKMC	muscle:	n/a
7	chr1:186649253-186649303	SKMC	muscle:	n/a
8	chr1:186649330-186649380	A549	lung:	n/a
9	chr1:186649153-186649203	HCPEpiC	choroid plexus:	n/a
10	chr1:186649253-186649303	AG09309	skin:	n/a
11	chr1:186649253-186649303	BJ	skin:	n/a
12	chr1:186649253-186649303	MCF-7	breast:	n/a
13	chr1:186649354-186649404	K562	blood:	n/a
14	chr1:186649354-186649404	GM12891	blood:	n/a
15	chr1:186649330-186649380	GM19239	blood:	n/a
16	chr1:186649153-186649203	AG09319	gingival:	n/a
17	chr1:186649253-186649303	HL-60	blood:	n/a
18	chr1:186649253-186649303	NB4	blood:	n/a
19	chr1:186649330-186649380	AG04450	lung:	fetal
20	chr1:186649354-186649404	NHBE	bronchial:	n/a
21	chr1:186649253-186649303	MCF10A-Er-Src	breast:	n/a
22	chr1:186649354-186649404	IMR90	lung:	fetal
23	chr1:186649330-186649380	NB4	blood:	n/a
24	chr1:186649153-186649203	HUVEC	blood vessel:	n/a
25	chr1:186649253-186649303	GM12891	blood:	n/a
26	chr1:186649354-186649404	PANC-1	pancreas:	n/a
27	chr1:186649153-186649203	HL-60	blood:	n/a
28	chr1:186649153-186649203	GM12878	blood:	n/a
29	chr1:186649253-186649303	HNPCEpiC	eye:	n/a
30	chr1:186649330-186649380	ProgFib	skin:	n/a
31	chr1:186649153-186649203	PFSK-1	brain:	n/a
32	chr1:186649253-186649303	LNCaP	prostate:	n/a
33	chr1:186649153-186649203	AG09309	skin:	n/a
34	chr1:186649253-186649303	HAEpiC	amniotic membrane:	n/a
35	chr1:186649354-186649404	HRE	kidney:	n/a
36	chr1:186649354-186649404	HCM	heart:	n/a
37	chr1:186649153-186649203	Hepatocyte	liver:	n/a
38	chr1:186649354-186649404	HMEC	breast:	n/a
39	chr1:186649330-186649380	CMK	blood:	n/a
40	chr1:186649153-186649203	GM12892	blood:	n/a
41	chr1:186649354-186649404	NB4	blood:	n/a
42	chr1:186649153-186649203	ProgFib	skin:	n/a
43	chr1:186649354-186649404	HNPCEpiC	eye:	n/a
44	chr1:186649153-186649203	SAEC	small airway:	n/a
45	chr1:186649153-186649203	NB4	blood:	n/a
46	chr1:186649253-186649303	HEK293	kidney:	embryo
47	chr1:186649153-186649203	SK-N-SH_RA	brain:	n/a
48	chr1:186649253-186649303	AG04449	skin:	fetal
49	chr1:186649330-186649380	NT2-D1	testis:	n/a
50	chr1:186649330-186649380	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:186648045..186648752-chr5:44808698..44809493,2	Hela-S3	cervix:
2	chr1:186649372..186649943-chr6:111136234..111137226,2	Hela-S3	cervix:
3	chr1:186649389..186649931-chr12:46766242..46766816,2	Hela-S3	cervix:
4	chr1:186641962..186644518-chr1:186645424..186648177,2	MCF-7	breast:
5	chr1:186646968..186647478-chr19:12903470..12904362,2	Hela-S3	cervix:
6	chr1:186649238..186650022-chr6:27860827..27861541,2	Hela-S3	cervix:
7	chr1:186649431..186649985-chr16:2014442..2015162,2	Hela-S3	cervix:
8	chr1:186648853..186649464-chr12:6875294..6876196,2	Hela-S3	cervix:

Variant related genes	Relation type
PTGS2	TF binding region
ENSG00000273129	TF binding region
PTGS2	CpG island
ENSG00000273129	CpG island
ENSG00000196331	chromatin interactions
ENSG00000255198	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000112996	chromatin interactions
ENSG00000159335	chromatin interactions
ENSG00000155111	chromatin interactions
ENSG00000140988	chromatin interactions
ENSG00000251141	chromatin interactions
ENSG00000233224	chromatin interactions

Extended variants
information (count: 179 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:179 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4648274	chr1:186646480-186646481	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531889788	chr1:186646491-186646492	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs183478129	chr1:186646503-186646504	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs16825748	chr1:186646544-186646545	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs571021619	chr1:186646560-186646561	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs4648273	chr1:186646578-186646579	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs4648272	chr1:186646587-186646588	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs186381971	chr1:186646590-186646591	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs11567825	chr1:186646594-186646595	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs66485939	chr1:186646596-186646597	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs536094537	chr1:186646667-186646668	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs529660282	chr1:186646691-186646692	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs4648271	chr1:186646693-186646694	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs200504288	chr1:186646734-186646735	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs113471898	chr1:186646744-186646745	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs191294326	chr1:186646746-186646747	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs375719557	chr1:186646762-186646763	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs20430	chr1:186646773-186646774	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs545853508	chr1:186646777-186646778	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs140664948	chr1:186646784-186646785	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs201592586	chr1:186646793-186646794	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs200311544	chr1:186646796-186646797	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs141500962	chr1:186646815-186646816	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs372267158	chr1:186646820-186646821	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs199735403	chr1:186646823-186646824	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs200316914	chr1:186646844-186646845	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs201493026	chr1:186646862-186646863	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs148479703	chr1:186646883-186646884	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs535541309	chr1:186646887-186646888	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs199513587	chr1:186646906-186646907	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs200842448	chr1:186646942-186646943	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs142741435	chr1:186646958-186646959	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs199612975	chr1:186646970-186646971	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs200719669	chr1:186646982-186646983	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs12759220	chr1:186647026-186647027	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs543317573	chr1:186647048-186647049	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs4648270	chr1:186647104-186647105	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs569282561	chr1:186647105-186647106	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs4648269	chr1:186647114-186647115	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs4648268	chr1:186647138-186647139	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs551607855	chr1:186647170-186647171	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs182375921	chr1:186647177-186647178	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs559155615	chr1:186647196-186647197	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs145859214	chr1:186647206-186647207	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs11567824	chr1:186647241-186647242	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs4648267	chr1:186647267-186647268	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs530566547	chr1:186647299-186647300	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs550484351	chr1:186647309-186647310	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs553869709	chr1:186647323-186647324	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs376809535	chr1:186647343-186647344	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	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
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Schizophrenia	19197363	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186632800-186649000	Weak transcription	Fetal Lung	lung
2	chr1:186639400-186648400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:186640200-186646600	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr1:186640200-186647800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:186640200-186647800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:186640800-186647800	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr1:186640800-186648000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr1:186640800-186648200	Weak transcription	Brain Angular Gyrus	brain
9	chr1:186640800-186649200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr1:186641400-186647600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:186641600-186647400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:186641600-186648400	Weak transcription	NHLF	lung
13	chr1:186641800-186648400	Weak transcription	Fetal Muscle Trunk	muscle
14	chr1:186642000-186646800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:186642200-186647000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:186642200-186647800	Strong transcription	HMEC	breast
17	chr1:186642200-186649200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:186642200-186649200	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr1:186642400-186649200	Weak transcription	Gastric	stomach
20	chr1:186642600-186648200	Weak transcription	Fetal Intestine Small	intestine
21	chr1:186642800-186647800	Strong transcription	NHEK	skin
22	chr1:186643000-186647800	Weak transcription	Fetal Intestine Large	intestine
23	chr1:186643400-186647000	Strong transcription	A549	lung
24	chr1:186643600-186646800	Strong transcription	Stomach Smooth Muscle	stomach
25	chr1:186643600-186647000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr1:186644000-186647600	Strong transcription	Duodenum Smooth Muscle	Duodenum
27	chr1:186644000-186648400	Weak transcription	Adipose Nuclei	Adipose
28	chr1:186644200-186649000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr1:186644200-186649000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:186644200-186649000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr1:186644200-186649200	Weak transcription	Lung	lung
32	chr1:186644400-186648400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr1:186644400-186649000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr1:186644400-186649200	Weak transcription	Aorta	Aorta
35	chr1:186644600-186648200	Weak transcription	Fetal Stomach	stomach
36	chr1:186644600-186648800	Weak transcription	Fetal Muscle Leg	muscle
37	chr1:186644600-186649000	Weak transcription	Ovary	ovary
38	chr1:186645200-186648000	Strong transcription	Osteobl	bone
39	chr1:186645400-186646800	Genic enhancers	HUVEC	blood vessel
40	chr1:186645800-186646600	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr1:186645800-186647800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr1:186645800-186647800	Weak transcription	Colon Smooth Muscle	Colon
43	chr1:186645800-186648400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr1:186645800-186649200	Weak transcription	Spleen	Spleen
45	chr1:186646000-186646800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr1:186646000-186647800	Weak transcription	NHDF-Ad	bronchial
47	chr1:186646000-186648200	Weak transcription	Rectal Smooth Muscle	rectum
48	chr1:186646000-186648200	Weak transcription	NH-A	brain
49	chr1:186646400-186647800	Genic enhancers	Hela-S3	cervix
50	chr1:186646400-186648400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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