Variant report

Variant	esv995050
Chromosome Location	chr1:228469242-228478757
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:164)
CpG islands
(count:611)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:164 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr1:228478246-228478656	K562	blood:	n/a	n/a
2	BHLHE40	chr1:228470655-228470974	K562	blood:	n/a	n/a
3	BHLHE40	chr1:228478177-228478579	K562	blood:	n/a	n/a
4	CBX3	chr1:228478137-228478644	K562	blood:	n/a	n/a
5	CCNT2	chr1:228478204-228478531	K562	blood:	n/a	chr1:228478388-228478408 chr1:228478324-228478344
6	CEBPB	chr1:228478236-228478624	K562	blood:	n/a	n/a
7	CEBPB	chr1:228478158-228478586	K562	blood:	n/a	n/a
8	CEBPD	chr1:228478195-228478561	K562	blood:	n/a	n/a
9	CEBPD	chr1:228478061-228478664	K562	blood:	n/a	n/a
10	CHD2	chr1:228478390-228478475	K562	blood:	n/a	n/a
11	CTCF	chr1:228470700-228470850	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr1:228477860-228478010	A549	lung:	n/a	n/a
13	CTCF	chr1:228470637-228470851	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr1:228470735-228470778	Gliobla	brain:	n/a	n/a
15	CTCF	chr1:228478145-228478333	K562	blood:	n/a	chr1:228478202-228478212
16	CTCF	chr1:228470743-228470783	A549	lung:	n/a	n/a
17	CTCF	chr1:228470760-228470910	K562	blood:	n/a	n/a
18	CTCF	chr1:228470620-228470910	K562	blood:	n/a	n/a
19	CTCF	chr1:228478180-228478330	HepG2	liver:	n/a	chr1:228478202-228478212
20	CTCF	chr1:228470606-228470885	K562	blood:	n/a	n/a
21	CTCF	chr1:228477943-228478135	K562	blood:	n/a	n/a
22	CTCF	chr1:228478036-228478334	T-47D	breast:	n/a	chr1:228478202-228478212
23	CTCF	chr1:228477940-228478090	HepG2	liver:	n/a	n/a
24	CTCF	chr1:228470667-228470878	K562	blood:	n/a	n/a
25	CTCF	chr1:228477940-228478090	K562	blood:	n/a	n/a
26	CTCF	chr1:228477729-228478481	K562	blood:	n/a	chr1:228478202-228478212
27	CTCF	chr1:228477836-228478418	K562	blood:	n/a	chr1:228478202-228478212
28	CTCF	chr1:228477914-228478337	HepG2	liver:	n/a	chr1:228478202-228478212
29	CTCF	chr1:228478000-228478150	K562	blood:	n/a	n/a
30	CTCF	chr1:228477900-228478050	GM12878	blood:	n/a	n/a
31	CTCF	chr1:228478170-228478256	Lung_OC	lung:	n/a	chr1:228478202-228478212
32	CTCF	chr1:228478081-228478428	T-47D	breast:	n/a	chr1:228478202-228478212
33	CTCF	chr1:228470700-228470850	K562	blood:	n/a	n/a
34	CTCF	chr1:228470640-228470790	HEK293	kidney:	n/a	n/a
35	CTCF	chr1:228477988-228478096	HepG2	liver:	n/a	n/a
36	CTCF	chr1:228470440-228470590	K562	blood:	n/a	n/a
37	CTCF	chr1:228478120-228478270	Caco-2	colon:	n/a	chr1:228478202-228478212
38	CTCF	chr1:228470656-228470866	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr1:228470569-228470853	K562	blood:	n/a	n/a
40	CTCF	chr1:228470677-228470835	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr1:228477960-228478110	HepG2	liver:	n/a	n/a
42	CTCF	chr1:228478040-228478190	AG09309	skin:	n/a	n/a
43	CTCF	chr1:228470640-228470790	GM12866	blood:	n/a	n/a
44	CTCF	chr1:228477866-228478411	K562	blood:	n/a	chr1:228478202-228478212
45	CTCF	chr1:228477911-228478393	K562	blood:	n/a	chr1:228478202-228478212
46	CTCF	chr1:228470485-228470894	K562	blood:	n/a	n/a
47	CTCF	chr1:228478000-228478150	A549	lung:	n/a	n/a
48	CTCF	chr1:228470779-228470783	Gliobla	brain:	n/a	n/a
49	CTCF	chr1:228470660-228470810	A549	lung:	n/a	n/a
50	CTCF	chr1:228477980-228478130	WI-38	lung:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228473980-228474030	MCF10A-Er-Src	breast:	n/a
2	chr1:228473980-228474030	MCF10A-Er-Src	breast:	n/a
3	chr1:228475463-228475513	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:228473933-228473983	GM12878	blood:	n/a
5	chr1:228470802-228470852	PANC-1	pancreas:	n/a
6	chr1:228473933-228473983	HPAEpiC	pulmonary alveolar:	n/a
7	chr1:228473933-228473983	HCF	heart:	n/a
8	chr1:228470904-228470954	NT2-D1	testis:	n/a
9	chr1:228477767-228477817	PrEC	prostate:	n/a
10	chr1:228470802-228470852	AG09309	skin:	n/a
11	chr1:228470802-228470852	HepG2	liver:	n/a
12	chr1:228477767-228477817	HEEpiC	esophagus:	n/a
13	chr1:228473704-228473754	HRPEpiC	eye:	n/a
14	chr1:228473704-228473754	HCT-116	colon:	n/a
15	chr1:228473980-228474030	SK-N-SH_RA	brain:	n/a
16	chr1:228473980-228474030	HEEpiC	esophagus:	n/a
17	chr1:228477767-228477817	BJ	skin:	n/a
18	chr1:228473781-228473831	BJ	skin:	n/a
19	chr1:228473781-228473831	K562	blood:	n/a
20	chr1:228475463-228475513	HNPCEpiC	eye:	n/a
21	chr1:228471009-228471059	HCM	heart:	n/a
22	chr1:228470802-228470852	HIPEpiC	eye:	n/a
23	chr1:228470802-228470852	SAEC	small airway:	n/a
24	chr1:228477767-228477817	PANC-1	pancreas:	n/a
25	chr1:228471009-228471059	T-47D	breast:	n/a
26	chr1:228471009-228471059	RPTEC	kidney:	n/a
27	chr1:228473933-228473983	HRCEpiC	kidney:	n/a
28	chr1:228477767-228477817	RPTEC	kidney:	n/a
29	chr1:228473873-228473923	PFSK-1	brain:	n/a
30	chr1:228471009-228471059	AG04450	lung:	fetal
31	chr1:228473704-228473754	HCPEpiC	choroid plexus:	n/a
32	chr1:228477767-228477817	HRPEpiC	eye:	n/a
33	chr1:228473704-228473754	NHDF-neo	bronchial:	n/a
34	chr1:228473933-228473983	ProgFib	skin:	n/a
35	chr1:228473704-228473754	Jurkat	blood:	n/a
36	chr1:228473873-228473923	A549	lung:	n/a
37	chr1:228473781-228473831	ProgFib	skin:	n/a
38	chr1:228475463-228475513	Jurkat	blood:	n/a
39	chr1:228473704-228473754	GM12891	blood:	n/a
40	chr1:228473873-228473923	HIPEpiC	eye:	n/a
41	chr1:228470904-228470954	SKMC	muscle:	n/a
42	chr1:228473980-228474030	GM12891	blood:	n/a
43	chr1:228477767-228477817	Jurkat	blood:	n/a
44	chr1:228473781-228473831	HAEpiC	amniotic membrane:	n/a
45	chr1:228473980-228474030	IMR90	lung:	fetal
46	chr1:228475463-228475513	NHDF-neo	bronchial:	n/a
47	chr1:228470904-228470954	HRPEpiC	eye:	n/a
48	chr1:228473781-228473831	HNPCEpiC	eye:	n/a
49	chr1:228473873-228473923	HNPCEpiC	eye:	n/a
50	chr1:228477767-228477817	HAEpiC	amniotic membrane:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228290994..228293117-chr1:228477432..228479388,2	K562	blood:
2	chr1:228463569..228466095-chr1:228472302..228475887,3	MCF-7	breast:
3	chr1:228476724..228479773-chr1:228482640..228484624,3	K562	blood:
4	chr1:228466929..228469506-chr1:228481575..228484301,2	MCF-7	breast:
5	chr1:228352843..228354997-chr1:228474222..228476055,2	K562	blood:
6	chr1:228467426..228469705-chr1:228474125..228476681,2	MCF-7	breast:
7	chr1:228474124..228476741-chr1:228593868..228595878,2	MCF-7	breast:
8	chr1:228474281..228476678-chr1:228493344..228496198,2	K562	blood:
9	chr1:228422838..228424736-chr1:228473654..228476445,2	MCF-7	breast:
10	chr1:228474588..228476521-chr1:228646417..228648380,2	K562	blood:
11	chr1:228478007..228479882-chr1:228496613..228498200,2	K562	blood:
12	chr1:228471019..228474213-chr1:228643868..228647117,3	MCF-7	breast:
13	chr1:228477052..228479311-chr1:228554955..228557444,2	K562	blood:
14	chr1:228267983..228269550-chr1:228473871..228475607,2	K562	blood:
15	chr1:228468187..228470207-chr1:228477251..228479949,2	K562	blood:
16	chr1:228469235..228472192-chr1:228496971..228498907,2	K562	blood:
17	chr1:228468318..228469993-chr1:228471813..228473827,2	K562	blood:
18	chr1:228477373..228479418-chr1:228539511..228541248,2	K562	blood:
19	chr1:228451031..228452706-chr1:228468801..228471254,2	K562	blood:
20	chr1:228380956..228383776-chr1:228470621..228473142,2	K562	blood:

No data

Variant related genes	Relation type
OBSCN	TF binding region
OBSCN	CpG island
ENSG00000231563	chromatin interactions
ENSG00000181873	chromatin interactions
ENSG00000154358	chromatin interactions
ENSG00000203684	chromatin interactions
ENSG00000181218	chromatin interactions
ENSG00000154370	chromatin interactions
ENSG00000269934	chromatin interactions
ENSG00000143793	chromatin interactions
ENSG00000196890	chromatin interactions

Extended variants
information (count: 560 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:560 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542409491	chr1:228469256-228469257	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs562165568	chr1:228469276-228469277	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs12059144	chr1:228469291-228469292	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs544565915	chr1:228469293-228469294	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs147947109	chr1:228469294-228469295	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs150761396	chr1:228469311-228469312	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs201755461	chr1:228469312-228469313	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs35152766	chr1:228469313-228469314	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs72513629	chr1:228469342-228469343	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs200035807	chr1:228469343-228469344	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs67543859	chr1:228469344-228469345	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs532010291	chr1:228469347-228469348	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs79292090	chr1:228469432-228469433	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs558987862	chr1:228469454-228469455	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs191964711	chr1:228469492-228469493	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547907742	chr1:228469496-228469497	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs370924710	chr1:228469528-228469529	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs184255547	chr1:228469542-228469543	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs550596341	chr1:228469555-228469556	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs373187851	chr1:228469589-228469590	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs570727941	chr1:228469593-228469594	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs147081875	chr1:228469622-228469623	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553420173	chr1:228469627-228469628	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561494847	chr1:228469629-228469630	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188531451	chr1:228469642-228469643	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376281341	chr1:228469664-228469665	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs151181660	chr1:228469674-228469675	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555866380	chr1:228469708-228469709	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140186693	chr1:228469720-228469721	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374614119	chr1:228469723-228469724	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368197891	chr1:228469731-228469732	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564579330	chr1:228469732-228469733	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs377649726	chr1:228469742-228469743	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200219027	chr1:228469752-228469753	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375216125	chr1:228469781-228469782	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150312546	chr1:228469801-228469802	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558899328	chr1:228469806-228469807	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528108008	chr1:228469812-228469813	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs3795784	chr1:228469821-228469822	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181194866	chr1:228469825-228469826	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs201052831	chr1:228469826-228469827	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs367748642	chr1:228469848-228469849	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372669133	chr1:228469851-228469852	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183888195	chr1:228469860-228469861	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189169421	chr1:228469861-228469862	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372024603	chr1:228469869-228469870	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs3795785	chr1:228469870-228469871	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs369366819	chr1:228469871-228469872	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74142687	chr1:228469873-228469874	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs376872596	chr1:228469878-228469879	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	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
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228455400-228484800	Weak transcription	A549	lung
2	chr1:228456400-228485800	Weak transcription	Hela-S3	cervix
3	chr1:228457200-228472000	Weak transcription	Fetal Heart	heart
4	chr1:228459800-228469600	Weak transcription	HSMMtube	muscle
5	chr1:228463800-228481400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:228464000-228472200	Weak transcription	Small Intestine	intestine
7	chr1:228464200-228470400	Weak transcription	HMEC	breast
8	chr1:228464200-228470600	Weak transcription	Aorta	Aorta
9	chr1:228464200-228473800	Weak transcription	Psoas Muscle	Psoas
10	chr1:228464200-228473800	Weak transcription	NHEK	skin
11	chr1:228464200-228478000	Strong transcription	Dnd41	blood
12	chr1:228464200-228491600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr1:228464400-228470600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr1:228464400-228470600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr1:228464400-228471800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr1:228464400-228472000	Genic enhancers	Skeletal Muscle Female	skeletal muscle
17	chr1:228464400-228473000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr1:228464400-228478400	Strong transcription	Thymus	Thymus
19	chr1:228464400-228479600	Weak transcription	Right Atrium	heart
20	chr1:228464400-228481400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr1:228464400-228482000	Weak transcription	Fetal Kidney	kidney
22	chr1:228464400-228489200	Strong transcription	Left Ventricle	heart
23	chr1:228464600-228470800	Weak transcription	Adipose Nuclei	Adipose
24	chr1:228464600-228473600	Weak transcription	Primary B cells from cord blood	blood
25	chr1:228464600-228475400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:228464600-228476800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:228464600-228481400	Weak transcription	Primary hematopoietic stem cells	blood
28	chr1:228464600-228483200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr1:228464600-228483200	Strong transcription	Fetal Intestine Small	intestine
30	chr1:228464600-228487000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr1:228464800-228472600	Strong transcription	Fetal Thymus	thymus
32	chr1:228464800-228476800	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr1:228464800-228477400	Strong transcription	Primary T cells from cord blood	blood
34	chr1:228465000-228469600	Strong transcription	Fetal Muscle Leg	muscle
35	chr1:228465000-228471800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:228465000-228472400	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr1:228465000-228476000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:228465000-228483600	Strong transcription	Right Ventricle	heart
39	chr1:228465000-228498000	Weak transcription	Fetal Brain Male	brain
40	chr1:228465200-228483400	Weak transcription	Colonic Mucosa	Colon
41	chr1:228465200-228483400	Strong transcription	Fetal Stomach	stomach
42	chr1:228465600-228474000	Weak transcription	Brain Anterior Caudate	brain
43	chr1:228465600-228483400	Strong transcription	Fetal Brain Female	brain
44	chr1:228465800-228476600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr1:228466200-228471600	Strong transcription	Placenta Amnion	Placenta Amnion
46	chr1:228466200-228471800	Strong transcription	Ovary	ovary
47	chr1:228466200-228472400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr1:228466200-228472600	Strong transcription	Brain Germinal Matrix	brain
49	chr1:228466200-228475800	Strong transcription	Fetal Intestine Large	intestine
50	chr1:228466200-228477200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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