Variant report

Variant	esv3436408
Chromosome Location	chr1:153894528-153895976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:780)
CpG islands
(count:794)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:780 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:153894525-153894675	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:153895552-153895878	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:153895475-153896162	K562	blood:	n/a	n/a
4	ATF1	chr1:153895430-153895788	K562	blood:	n/a	n/a
5	ATF2	chr1:153895530-153896284	GM12878	blood:	n/a	n/a
6	ATF2	chr1:153895505-153896208	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:153895496-153896129	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:153895430-153896376	GM12878	blood:	n/a	n/a
9	ATF3	chr1:153895561-153896100	A549	lung:	n/a	n/a
10	BACH1	chr1:153895465-153896537	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:153895679-153896291	K562	blood:	n/a	n/a
12	BCL3	chr1:153895472-153896312	A549	lung:	n/a	chr1:153895828-153895837
13	BCL3	chr1:153895488-153896193	A549	lung:	n/a	chr1:153895828-153895837
14	BCLAF1	chr1:153895524-153896181	GM12878	blood:	n/a	chr1:153895828-153895837
15	BCLAF1	chr1:153895432-153896352	GM12878	blood:	n/a	chr1:153895828-153895837
16	BHLHE40	chr1:153895094-153895240	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:153895520-153896225	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:153894255-153894750	K562	blood:	n/a	n/a
19	BHLHE40	chr1:153895088-153895191	K562	blood:	n/a	n/a
20	BHLHE40	chr1:153895530-153896398	K562	blood:	n/a	n/a
21	BRCA1	chr1:153895503-153896151	GM12878	blood:	n/a	n/a
22	BRCA1	chr1:153895801-153896090	HepG2	liver:	n/a	n/a
23	BRCA1	chr1:153895134-153896731	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr1:153895560-153896100	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr1:153895005-153896297	K562	blood:	n/a	n/a
26	CCNT2	chr1:153894520-153896218	K562	blood:	n/a	chr1:153895326-153895335 chr1:153895016-153895025
27	CEBPB	chr1:153895482-153896377	GM12878	blood:	n/a	n/a
28	CEBPB	chr1:153895700-153896024	GM12878	blood:	n/a	n/a
29	CEBPB	chr1:153895502-153896000	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:153895648-153895997	HepG2	liver:	n/a	n/a
31	CEBPD	chr1:153895466-153895947	HepG2	liver:	n/a	n/a
32	CEBPZ	chr1:153895426-153895774	HepG2	liver:	n/a	n/a
33	CHD1	chr1:153894423-153894703	GM12878	blood:	n/a	n/a
34	CHD1	chr1:153895786-153896117	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr1:153895629-153896633	GM12878	blood:	n/a	n/a
36	CHD2	chr1:153894963-153896212	HepG2	liver:	n/a	chr1:153895015-153895025
37	CHD2	chr1:153894987-153896377	H1-hESC	embryonic stem cell:	n/a	chr1:153895015-153895025
38	CHD2	chr1:153894813-153896236	K562	blood:	n/a	chr1:153895015-153895025
39	CHD2	chr1:153894942-153896410	GM12878	blood:	n/a	chr1:153895015-153895025
40	CHD2	chr1:153894567-153896341	Hela-S3	cervix:	n/a	chr1:153895015-153895025
41	CREB1	chr1:153894885-153895998	GM12878	blood:	n/a	n/a
42	CREB1	chr1:153895410-153895822	A549	lung:	n/a	n/a
43	CREB1	chr1:153895246-153895827	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr1:153895205-153896001	A549	lung:	n/a	n/a
45	CTCF	chr1:153895100-153895250	GM12874	blood:	n/a	n/a
46	CTCF	chr1:153895120-153895270	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr1:153895120-153895270	GM12865	blood:	n/a	n/a
48	CTCF	chr1:153895098-153895290	GM19240	blood:	n/a	n/a
49	CTCF	chr1:153895140-153895290	GM12871	blood:	n/a	n/a
50	CTCF	chr1:153895120-153895270	AG09319	gingival:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153895885-153895935	HIPEpiC	eye:	n/a
2	chr1:153895885-153895935	HIPEpiC	eye:	n/a
3	chr1:153895721-153895771	AG10803	skin:	n/a
4	chr1:153895546-153895596	HEK293	kidney:	embryo
5	chr1:153895324-153895374	HAEpiC	amniotic membrane:	n/a
6	chr1:153895881-153895931	HRCEpiC	kidney:	n/a
7	chr1:153895881-153895931	Caco-2	colon:	n/a
8	chr1:153895721-153895771	H1-hESC	embryonic stem cell:	embryo
9	chr1:153895324-153895374	HepG2	liver:	n/a
10	chr1:153895885-153895935	GM12891	blood:	n/a
11	chr1:153895881-153895931	AoSMC	blood vessel:	n/a
12	chr1:153895721-153895771	BJ	skin:	n/a
13	chr1:153895721-153895771	GM12878	blood:	n/a
14	chr1:153895177-153895227	HepG2	liver:	n/a
15	chr1:153895324-153895374	ovcar-3	ovarian:	n/a
16	chr1:153894941-153894991	Hela-S3	cervix:	n/a
17	chr1:153895448-153895498	PrEC	prostate:	n/a
18	chr1:153895177-153895227	SK-N-SH_RA	brain:	n/a
19	chr1:153894941-153894991	GM12892	blood:	n/a
20	chr1:153895961-153896011	RPTEC	kidney:	n/a
21	chr1:153895607-153895657	K562	blood:	n/a
22	chr1:153895398-153895448	HAEpiC	amniotic membrane:	n/a
23	chr1:153895888-153895938	SK-N-SH_RA	brain:	n/a
24	chr1:153894579-153894629	Caco-2	colon:	n/a
25	chr1:153894579-153894629	A549	lung:	n/a
26	chr1:153895885-153895935	HRPEpiC	eye:	n/a
27	chr1:153895881-153895931	Hela-S3	cervix:	n/a
28	chr1:153895398-153895448	RPTEC	kidney:	n/a
29	chr1:153895607-153895657	A549	lung:	n/a
30	chr1:153895721-153895771	HRE	kidney:	n/a
31	chr1:153894579-153894629	Jurkat	blood:	n/a
32	chr1:153894579-153894629	AG04449	skin:	fetal
33	chr1:153895324-153895374	AG09319	gingival:	n/a
34	chr1:153895607-153895657	Jurkat	blood:	n/a
35	chr1:153894579-153894629	HepG2	liver:	n/a
36	chr1:153895607-153895657	AG04450	lung:	fetal
37	chr1:153895324-153895374	HRCEpiC	kidney:	n/a
38	chr1:153895881-153895931	HepG2	liver:	n/a
39	chr1:153895885-153895935	BE2_C	brain:	n/a
40	chr1:153895961-153896011	IMR90	lung:	fetal
41	chr1:153895324-153895374	Hela-S3	cervix:	n/a
42	chr1:153895448-153895498	AG09309	skin:	n/a
43	chr1:153894579-153894629	AoSMC	blood vessel:	n/a
44	chr1:153895607-153895657	AG10803	skin:	n/a
45	chr1:153895546-153895596	PFSK-1	brain:	n/a
46	chr1:153895448-153895498	Hepatocyte	liver:	n/a
47	chr1:153895177-153895227	Jurkat	blood:	n/a
48	chr1:153895546-153895596	SKMC	muscle:	n/a
49	chr1:153895546-153895596	IMR90	lung:	fetal
50	chr1:153894579-153894629	NHBE	bronchial:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:153699430..153701547-chr1:153893565..153895608,2	MCF-7	breast:
2	chr1:153858733..153861625-chr1:153893307..153895024,2	K562	blood:
3	chr1:153892664..153896587-chr1:153948190..153951187,6	K562	blood:
4	chr1:153759800..153761704-chr1:153893842..153895431,2	K562	blood:
5	chr1:153895003..153895633-chr10:70166494..70167290,2	Hela-S3	cervix:
6	chr1:153895897..153896422-chr11:48153597..48154395,2	Hela-S3	cervix:
7	chr1:153754212..153755933-chr1:153895678..153897558,2	MCF-7	breast:
8	chr1:153892719..153895039-chr1:153953793..153956278,2	K562	blood:
9	chr1:153893510..153896669-chr1:153958441..153960611,3	K562	blood:
10	chr1:153883515..153885221-chr1:153892964..153894776,3	MCF-7	breast:
11	chr1:153890756..153897034-chr1:153961597..153964863,14	K562	blood:
12	chr1:153895740..153897837-chr1:153943889..153946468,2	K562	blood:
13	chr1:153894942..153895704-chr1:153918773..153919666,3	K562	blood:
14	chr1:153895633..153896175-chr1:153949945..153950661,2	Hela-S3	cervix:
15	chr1:153876373..153878542-chr1:153895885..153898675,2	MCF-7	breast:
16	chr1:153877108..153878682-chr1:153895765..153897266,2	MCF-7	breast:
17	chr1:153537683..153540046-chr1:153895076..153896651,2	K562	blood:
18	chr1:153747665..153750002-chr1:153895693..153897209,2	MCF-7	breast:
19	chr1:153746879..153748867-chr1:153894033..153896594,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CREB3L4-1	chr1:153895762-153896438	NONHSAT006552

No data

Variant related genes	Relation type
GATAD2B	TF binding region
GATAD2B	CpG island
ENSG00000143545	chromatin interactions
ENSG00000143624	chromatin interactions
ENSG00000143554	chromatin interactions
ENSG00000196754	chromatin interactions
ENSG00000177954	chromatin interactions
ENSG00000272654	chromatin interactions
ENSG00000198837	chromatin interactions
ENSG00000143543	chromatin interactions
ENSG00000204130	chromatin interactions

Extended variants
information (count: 39 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:39 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553602363	chr1:153894603-153894604	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs565741605	chr1:153894604-153894605	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs539649462	chr1:153894623-153894624	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs148732990	chr1:153894665-153894666	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs576293210	chr1:153894686-153894687	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs372072815	chr1:153894693-153894694	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs142336459	chr1:153894711-153894712	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs570451535	chr1:153894764-153894765	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs529245593	chr1:153894775-153894776	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs151287239	chr1:153894821-153894822	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs573982684	chr1:153894828-153894829	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs541378618	chr1:153894930-153894931	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs559611914	chr1:153894958-153894959	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs533205400	chr1:153895198-153895199	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs545091403	chr1:153895223-153895224	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs563588960	chr1:153895305-153895306	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs530990577	chr1:153895516-153895517	Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs140541322	chr1:153895547-153895548	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs576737972	chr1:153895550-153895551	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs111228526	chr1:153895581-153895582	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs147097629	chr1:153895628-153895629	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs537442262	chr1:153895654-153895655	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs528904703	chr1:153895662-153895663	Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs547323062	chr1:153895718-153895719	Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs187886056	chr1:153895734-153895735	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs539581606	chr1:153895765-153895766	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
27	rs147736979	chr1:153895778-153895779	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
28	rs569893296	chr1:153895796-153895797	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
29	rs537227871	chr1:153895817-153895818	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
30	rs555386612	chr1:153895818-153895819	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
31	rs573850190	chr1:153895848-153895849	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
32	rs542943478	chr1:153895861-153895862	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
33	rs534709962	chr1:153895869-153895870	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
34	rs553290218	chr1:153895877-153895878	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
35	rs577613688	chr1:153895884-153895885	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
36	rs545126292	chr1:153895889-153895890	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
37	rs76474450	chr1:153895936-153895937	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
38	rs575451467	chr1:153895942-153895943	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
39	rs12032520	chr1:153895953-153895954	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:114)

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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	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
Non-syndromic sensorineural hearing loss	15273396	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
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
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
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
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Liver carcinoma	19366792	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153891600-153894800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:153892200-153894600	Flanking Active TSS	Primary hematopoietic stem cells	blood
3	chr1:153892400-153894600	Flanking Active TSS	Primary T cells from cord blood	blood
4	chr1:153892400-153894600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
5	chr1:153892400-153894600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr1:153892400-153894600	Transcr. at gene 5' and 3'	Dnd41	blood
7	chr1:153892400-153895000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:153892600-153894800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr1:153892600-153894800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr1:153892600-153894800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr1:153892800-153894600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
12	chr1:153892800-153894600	Flanking Active TSS	Brain Cingulate Gyrus	brain
13	chr1:153892800-153894600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr1:153892800-153894800	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr1:153893000-153894600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
16	chr1:153893000-153894600	Flanking Active TSS	Fetal Lung	lung
17	chr1:153893000-153894600	Flanking Active TSS	Stomach Smooth Muscle	stomach
18	chr1:153893000-153894600	Flanking Active TSS	HUVEC	blood vessel
19	chr1:153893200-153894600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
20	chr1:153893200-153894600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
21	chr1:153893200-153894600	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
22	chr1:153893200-153894800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
23	chr1:153893200-153894800	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr1:153893200-153896200	Active TSS	NHDF-Ad	bronchial
25	chr1:153893400-153894600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
26	chr1:153893400-153894600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
27	chr1:153893400-153894600	Flanking Active TSS	Osteobl	bone
28	chr1:153893600-153894600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr1:153893600-153894600	Flanking Active TSS	Brain Substantia Nigra	brain
30	chr1:153893600-153894600	Flanking Active TSS	Duodenum Mucosa	Duodenum
31	chr1:153893600-153894800	Flanking Active TSS	Liver	Liver
32	chr1:153893600-153894800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
33	chr1:153893600-153896400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr1:153893600-153897000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr1:153893800-153894800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
36	chr1:153893800-153896000	Active TSS	NHLF	lung
37	chr1:153893800-153896200	Active TSS	HSMMtube	muscle
38	chr1:153893800-153896200	Active TSS	K562	blood
39	chr1:153893800-153896400	Active TSS	H1 Cell Line	embryonic stem cell
40	chr1:153893800-153896400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:153893800-153896400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:153893800-153896600	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr1:153893800-153896800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:153893800-153896800	Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr1:153893800-153896800	Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr1:153893800-153896800	Active TSS	Pancreatic Islets	Pancreatic Islet
47	chr1:153893800-153897000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:153893800-153897400	Active TSS	H9 Cell Line	embryonic stem cell
49	chr1:153894000-153894600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr1:153894000-153894600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood

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