Variant report

Variant	nsv548404
Chromosome Location	chr1:186647104-186649308
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	chr1:186649029-186650035	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
5	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
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	chr1:186649073-186650354	Hela-S3	cervix:	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	chr1:186649223-186650014	ECC-1	luminal epithelium:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
11	CEBPB	chr1:186649254-186650099	A549	lung:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
12	CEBPB	chr1:186649165-186649952	HCT-116	colon:	n/a	chr1:186649680-186649689 chr1:186649678-186649691 chr1:186649680-186649689 chr1:186649680-186649689
13	CHD2	chr1:186649176-186650578	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr1:186649308-186649674	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr1:186649137-186649803	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr1:186649218-186649743	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr1:186649244-186649965	A549	lung:	n/a	n/a
18	CTBP2	chr1:186649204-186650086	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr1:186649306-186649309	Fibrobl	skin:	n/a	n/a
20	CTCF	chr1:186649210-186649769	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:186649289-186649559	T-47D	breast:	n/a	n/a
22	CTCF	chr1:186649298-186649614	GM13976	blood:	n/a	n/a
23	CTCF	chr1:186649285-186649610	GM12892	blood:	n/a	n/a
24	CTCF	chr1:186649201-186649622	GM19240	blood:	n/a	n/a
25	CTCF	chr1:186649295-186649623	GM13977	blood:	n/a	n/a
26	CTCF	chr1:186649140-186649290	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr1:186649290-186649596	GM10266	blood:	n/a	n/a
28	CTCF	chr1:186649251-186649625	MCF-7	breast:	n/a	n/a
29	CTCF	chr1:186649227-186649643	A549	lung:	n/a	n/a
30	CTCF	chr1:186649286-186649679	A549	lung:	n/a	n/a
31	CTCF	chr1:186649291-186649620	MCF-7	breast:	n/a	n/a
32	CTCF	chr1:186649250-186649618	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:186649220-186649731	A549	lung:	n/a	n/a
34	CTCF	chr1:186649308-186649631	ProgFib	skin:	n/a	n/a
35	CTCF	chr1:186649205-186649591	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr1:186649158-186649618	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr1:186649262-186649632	MCF-7	breast:	n/a	n/a
38	CTCF	chr1:186649282-186649619	GM12891	blood:	n/a	n/a
39	CTCF	chr1:186649256-186649632	GM19238	blood:	n/a	n/a
40	CTCF	chr1:186649244-186649661	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:186648686-186651449	A549	lung:	n/a	chr1:186651134-186651142
42	CTCF	chr1:186649207-186649815	IMR90	lung:	n/a	n/a
43	CTCF	chr1:186649296-186649604	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr1:186649269-186649630	NHEK	skin:	n/a	n/a
45	CTCF	chr1:186649250-186649634	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:186649295-186649690	GM12878	blood:	n/a	n/a
47	E2F1	chr1:186649173-186649870	Hela-S3	cervix:	n/a	chr1:186649353-186649363
48	E2F4	chr1:186649239-186649935	MCF10A-Er-Src	breast:	n/a	chr1:186649353-186649363
49	E2F6	chr1:186649189-186650300	A549	lung:	n/a	chr1:186650004-186650016 chr1:186650008-186650018 chr1:186650011-186650021 chr1:186649353-186649363
50	ELF1	chr1:186649300-186649864	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:186649153-186649203	HRE	kidney:	n/a
2	chr1:186649253-186649303	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:186649253-186649303	AoSMC	blood vessel:	n/a
4	chr1:186649153-186649203	H1-hESC	embryonic stem cell:	embryo
5	chr1:186649153-186649203	ProgFib	skin:	n/a
6	chr1:186649253-186649303	HepG2	liver:	n/a
7	chr1:186649253-186649303	U87	brain:	n/a
8	chr1:186649153-186649203	AG04450	lung:	fetal
9	chr1:186649253-186649303	SK-N-SH	brain:	n/a
10	chr1:186649253-186649303	T-47D	breast:	n/a
11	chr1:186649153-186649203	HAEpiC	amniotic membrane:	n/a
12	chr1:186649153-186649203	GM06990	blood:	n/a
13	chr1:186649153-186649203	HIPEpiC	eye:	n/a
14	chr1:186649253-186649303	HCT-116	colon:	n/a
15	chr1:186649253-186649303	HCF	heart:	n/a
16	chr1:186649253-186649303	IMR90	lung:	fetal
17	chr1:186649253-186649303	HUVEC	blood vessel:	n/a
18	chr1:186649153-186649203	SAEC	small airway:	n/a
19	chr1:186649253-186649303	AG04450	lung:	fetal
20	chr1:186649253-186649303	ovcar-3	ovarian:	n/a
21	chr1:186649253-186649303	AG09319	gingival:	n/a
22	chr1:186649253-186649303	GM12891	blood:	n/a
23	chr1:186649153-186649203	HUVEC	blood vessel:	n/a
24	chr1:186649153-186649203	Jurkat	blood:	n/a
25	chr1:186649253-186649303	HRE	kidney:	n/a
26	chr1:186649153-186649203	RPTEC	kidney:	n/a
27	chr1:186649153-186649203	CMK	blood:	n/a
28	chr1:186649153-186649203	AoSMC	blood vessel:	n/a
29	chr1:186649153-186649203	PrEC	prostate:	n/a
30	chr1:186649153-186649203	K562	blood:	n/a
31	chr1:186649153-186649203	HEK293	kidney:	embryo
32	chr1:186649153-186649203	AG09319	gingival:	n/a
33	chr1:186649253-186649303	NH-A	brain:	n/a
34	chr1:186649253-186649303	HNPCEpiC	eye:	n/a
35	chr1:186649253-186649303	H1-hESC	embryonic stem cell:	embryo
36	chr1:186649253-186649303	HEK293	kidney:	embryo
37	chr1:186649153-186649203	SK-N-SH_RA	brain:	n/a
38	chr1:186649253-186649303	A549	lung:	n/a
39	chr1:186649153-186649203	HRPEpiC	eye:	n/a
40	chr1:186649253-186649303	CMK	blood:	n/a
41	chr1:186649253-186649303	PANC-1	pancreas:	n/a
42	chr1:186649253-186649303	Hela-S3	cervix:	n/a
43	chr1:186649153-186649203	ovcar-3	ovarian:	n/a
44	chr1:186649153-186649203	HCM	heart:	n/a
45	chr1:186649253-186649303	ECC-1	luminal epithelium:	n/a
46	chr1:186649253-186649303	BJ	skin:	n/a
47	chr1:186649253-186649303	HEEpiC	esophagus:	n/a
48	chr1:186649253-186649303	PFSK-1	brain:	n/a
49	chr1:186649253-186649303	NB4	blood:	n/a
50	chr1:186649153-186649203	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:186648853..186649464-chr12:6875294..6876196,2	Hela-S3	cervix:
2	chr1:186646968..186647478-chr19:12903470..12904362,2	Hela-S3	cervix:
3	chr1:186648045..186648752-chr5:44808698..44809493,2	Hela-S3	cervix:
4	chr1:186641962..186644518-chr1:186645424..186648177,2	MCF-7	breast:
5	chr1:186649238..186650022-chr6:27860827..27861541,2	Hela-S3	cervix:

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

Extended variants
information (count: 119 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:119 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	rs201605778	chr1:186647345-186647346	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	rs200093261	chr1:186647351-186647352	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	rs200589642	chr1:186647363-186647364	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	rs201432087	chr1:186647369-186647370	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	rs4648266	chr1:186647384-186647385	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
20	rs201238353	chr1:186647412-186647413	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	rs536033236	chr1:186647413-186647414	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	rs4648265	chr1:186647418-186647419	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
23	rs199972508	chr1:186647430-186647431	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	rs200911813	chr1:186647439-186647440	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	rs201938310	chr1:186647448-186647449	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	rs566984593	chr1:186647452-186647453	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	rs4648264	chr1:186647454-186647455	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
28	rs20429	chr1:186647460-186647461	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	rs539933723	chr1:186647469-186647470	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	rs202013754	chr1:186647478-186647479	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	rs200314986	chr1:186647484-186647485	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	rs377655174	chr1:186647506-186647507	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	rs557821908	chr1:186647532-186647533	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	rs201583472	chr1:186647543-186647544	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	rs199732850	chr1:186647547-186647548	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	rs200569874	chr1:186647559-186647560	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	rs200581318	chr1:186647571-186647572	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	rs201084591	chr1:186647585-186647586	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	rs537089358	chr1:186647605-186647606	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs555227121	chr1:186647607-186647608	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs20428	chr1:186647609-186647610	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs4987012	chr1:186647615-186647616	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs540833742	chr1:186647629-186647630	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs567471068	chr1:186647651-186647652	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs577618382	chr1:186647653-186647654	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs545082358	chr1:186647661-186647662	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs563412199	chr1:186647708-186647709	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs530500830	chr1:186647745-186647746	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs367780231	chr1:186647782-186647783	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs549025257	chr1:186647804-186647805	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Strong transcription	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:221 , 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	chr1:186640200-186647800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr1:186640200-186647800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:186640800-186647800	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr1:186640800-186648000	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr1:186640800-186648200	Weak transcription	Brain Angular Gyrus	brain
8	chr1:186640800-186649200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr1:186641400-186647600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:186641600-186647400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:186641600-186648400	Weak transcription	NHLF	lung
12	chr1:186641800-186648400	Weak transcription	Fetal Muscle Trunk	muscle
13	chr1:186642200-186647800	Strong transcription	HMEC	breast
14	chr1:186642200-186649200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:186642200-186649200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr1:186642400-186649200	Weak transcription	Gastric	stomach
17	chr1:186642600-186648200	Weak transcription	Fetal Intestine Small	intestine
18	chr1:186642800-186647800	Strong transcription	NHEK	skin
19	chr1:186643000-186647800	Weak transcription	Fetal Intestine Large	intestine
20	chr1:186644000-186647600	Strong transcription	Duodenum Smooth Muscle	Duodenum
21	chr1:186644000-186648400	Weak transcription	Adipose Nuclei	Adipose
22	chr1:186644200-186649000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr1:186644200-186649000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr1:186644200-186649000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr1:186644200-186649200	Weak transcription	Lung	lung
26	chr1:186644400-186648400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:186644400-186649000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:186644400-186649200	Weak transcription	Aorta	Aorta
29	chr1:186644600-186648200	Weak transcription	Fetal Stomach	stomach
30	chr1:186644600-186648800	Weak transcription	Fetal Muscle Leg	muscle
31	chr1:186644600-186649000	Weak transcription	Ovary	ovary
32	chr1:186645200-186648000	Strong transcription	Osteobl	bone
33	chr1:186645800-186647800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:186645800-186647800	Weak transcription	Colon Smooth Muscle	Colon
35	chr1:186645800-186648400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr1:186645800-186649200	Weak transcription	Spleen	Spleen
37	chr1:186646000-186647800	Weak transcription	NHDF-Ad	bronchial
38	chr1:186646000-186648200	Weak transcription	Rectal Smooth Muscle	rectum
39	chr1:186646000-186648200	Weak transcription	NH-A	brain
40	chr1:186646400-186647800	Genic enhancers	Hela-S3	cervix
41	chr1:186646400-186648400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:186646400-186651000	Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr1:186646600-186648000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr1:186646600-186648200	Genic enhancers	Primary neutrophils fromperipheralblood	blood
45	chr1:186646800-186647600	Transcr. at gene 5' and 3'	HUVEC	blood vessel
46	chr1:186646800-186647800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr1:186646800-186649200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:186647000-186647600	Weak transcription	A549	lung
49	chr1:186647000-186647800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr1:186647000-186647800	Strong transcription	Monocytes-CD14+_RO01746	blood

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