Variant report

Variant	esv1793882
Chromosome Location	chr1:158961777-158972490
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	ATF2	chr1:158969408-158969884	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr1:158969462-158969881	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr1:158966132-158966379	GM12878	blood:	n/a	n/a
4	BATF	chr1:158966067-158966420	GM12878	blood:	n/a	n/a
5	BCL11A	chr1:158966081-158966327	GM12878	blood:	n/a	n/a
6	BCLAF1	chr1:158966155-158966402	GM12878	blood:	n/a	n/a
7	BCLAF1	chr1:158968542-158968880	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:158968486-158968864	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:158966157-158966444	GM12878	blood:	n/a	n/a
10	BRCA1	chr1:158969378-158971208	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr1:158970050-158970250	K562	blood:	n/a	n/a
12	CEBPB	chr1:158969455-158970765	Hela-S3	cervix:	n/a	chr1:158969611-158969623
13	CEBPB	chr1:158969405-158969862	H1-hESC	embryonic stem cell:	n/a	chr1:158969611-158969623
14	CHD2	chr1:158970393-158970769	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr1:158966232-158966388	GM12878	blood:	n/a	n/a
16	CHD2	chr1:158969217-158970014	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr1:158969483-158969898	Hela-S3	cervix:	n/a	n/a
18	CREB1	chr1:158969485-158969929	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTBP2	chr1:158969464-158969922	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr1:158968574-158968775	GM20000	blood:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
21	CTCF	chr1:158968532-158968791	ECC-1	luminal epithelium:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
22	CTCF	chr1:158968522-158968797	Gliobla	brain:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
23	CTCF	chr1:158968580-158968730	SK-N-SH_RA	brain:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
24	CTCF	chr1:158968616-158968689	GM19240	blood:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
25	CTCF	chr1:158968409-158968857	HepG2	liver:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
26	CTCF	chr1:158968600-158968750	MCF-7	breast:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
27	CTCF	chr1:158968580-158968730	GM06990	blood:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
28	CTCF	chr1:158968620-158968770	Caco-2	colon:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
29	CTCF	chr1:158968580-158968730	HUVEC	blood vessel:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
30	CTCF	chr1:158968580-158968730	HEK293	kidney:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
31	CTCF	chr1:158968600-158968750	HPF	lung:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
32	CTCF	chr1:158968585-158968707	GM19239	blood:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
33	CTCF	chr1:158968560-158968710	RPTEC	kidney:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
34	CTCF	chr1:158968471-158968895	MCF-7	breast:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
35	CTCF	chr1:158968600-158968750	WERI-Rb-1	eye:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
36	CTCF	chr1:158968560-158968710	AoAF	blood vessel:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
37	CTCF	chr1:158968620-158968770	GM12864	blood:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
38	CTCF	chr1:158968543-158968771	MCF-7	breast:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
39	CTCF	chr1:158968840-158968990	WI-38	lung:	n/a	n/a
40	CTCF	chr1:158968330-158968942	IMR90	lung:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
41	CTCF	chr1:158968535-158968783	Hela-S3	cervix:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
42	CTCF	chr1:158968580-158968730	GM12874	blood:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
43	CTCF	chr1:158968524-158968735	HepG2	liver:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
44	CTCF	chr1:158969360-158969510	HMF	breast:	n/a	n/a
45	CTCF	chr1:158968580-158968730	RPTEC	kidney:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
46	CTCF	chr1:158968640-158968790	NHEK	skin:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
47	CTCF	chr1:158968580-158968730	HCT-116	colon:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
48	CTCF	chr1:158968600-158968750	GM12865	blood:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
49	CTCF	chr1:158968600-158968750	HepG2	liver:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668
50	CTCF	chr1:158968544-158968820	GM10266	blood:	n/a	chr1:158968651-158968669 chr1:158968646-158968667 chr1:158968653-158968666 chr1:158968652-158968668

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158969712-158969762	HAEpiC	amniotic membrane:	n/a
2	chr1:158969712-158969762	NHDF-neo	bronchial:	n/a
3	chr1:158969712-158969762	IMR90	lung:	fetal
4	chr1:158969712-158969762	MCF10A-Er-Src	breast:	n/a
5	chr1:158969712-158969762	ProgFib	skin:	n/a
6	chr1:158969712-158969762	MCF-7	breast:	n/a
7	chr1:158969712-158969762	NHBE	bronchial:	n/a
8	chr1:158969712-158969762	AoSMC	blood vessel:	n/a
9	chr1:158969712-158969762	H1-hESC	embryonic stem cell:	embryo
10	chr1:158969712-158969762	HEEpiC	esophagus:	n/a
11	chr1:158969712-158969762	AG10803	skin:	n/a
12	chr1:158969712-158969762	HMEC	breast:	n/a
13	chr1:158969712-158969762	AG09309	skin:	n/a
14	chr1:158969712-158969762	HEK293	kidney:	embryo
15	chr1:158969712-158969762	BE2_C	brain:	n/a
16	chr1:158969712-158969762	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:158969712-158969762	NB4	blood:	n/a
18	chr1:158969712-158969762	PFSK-1	brain:	n/a
19	chr1:158969712-158969762	LNCaP	prostate:	n/a
20	chr1:158969712-158969762	Caco-2	colon:	n/a
21	chr1:158969712-158969762	AG04449	skin:	fetal
22	chr1:158969712-158969762	RPTEC	kidney:	n/a
23	chr1:158969712-158969762	CMK	blood:	n/a
24	chr1:158969712-158969762	PANC-1	pancreas:	n/a
25	chr1:158969712-158969762	NT2-D1	testis:	n/a
26	chr1:158969712-158969762	HRPEpiC	eye:	n/a
27	chr1:158969712-158969762	SKMC	muscle:	n/a
28	chr1:158969712-158969762	HCT-116	colon:	n/a
29	chr1:158969712-158969762	NH-A	brain:	n/a
30	chr1:158969712-158969762	SK-N-SH_RA	brain:	n/a
31	chr1:158969712-158969762	ECC-1	luminal epithelium:	n/a
32	chr1:158969712-158969762	Hela-S3	cervix:	n/a
33	chr1:158969712-158969762	HCF	heart:	n/a
34	chr1:158969712-158969762	GM12892	blood:	n/a
35	chr1:158969712-158969762	AG09319	gingival:	n/a
36	chr1:158969712-158969762	GM12878	blood:	n/a
37	chr1:158969712-158969762	A549	lung:	n/a
38	chr1:158969712-158969762	PrEC	prostate:	n/a
39	chr1:158969712-158969762	AG04450	lung:	fetal
40	chr1:158969712-158969762	SK-N-MC	brain:	n/a
41	chr1:158969712-158969762	K562	blood:	n/a
42	chr1:158969712-158969762	HL-60	blood:	n/a
43	chr1:158969712-158969762	GM19239	blood:	n/a
44	chr1:158969712-158969762	ovcar-3	ovarian:	n/a
45	chr1:158969712-158969762	HIPEpiC	eye:	n/a
46	chr1:158969712-158969762	GM06990	blood:	n/a
47	chr1:158969712-158969762	GM12891	blood:	n/a
48	chr1:158969712-158969762	HCM	heart:	n/a
49	chr1:158969712-158969762	Jurkat	blood:	n/a
50	chr1:158969712-158969762	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:158475878..158476640-chr1:158968361..158968916,3	MCF-7	breast:
2	chr1:158970577..158973262-chr1:158975751..158977296,2	K562	blood:
3	chr1:158970353..158971192-chr3:169482441..169483092,2	Hela-S3	cervix:
4	chr1:158768206..158768907-chr1:158968540..158969106,3	MCF-7	breast:
5	chr1:158968169..158968975-chr1:159041872..159042414,2	K562	blood:
6	chr1:158763178..158764363-chr1:158967947..158968721,3	MCF-7	breast:
7	chr1:158476296..158476820-chr1:158968188..158969128,2	K562	blood:
8	chr1:158173526..158174221-chr1:158968084..158968716,3	MCF-7	breast:
9	chr1:158954353..158956986-chr1:158959866..158962635,3	K562	blood:
10	chr1:158954353..158956986-chr1:158959866..158962393,2	K562	blood:
11	chr1:158640177..158642154-chr1:158966970..158969167,2	K562	blood:

Variant related genes	Relation type
IFI16	TF binding region
IFI16	CpG island
ENSG00000176320	chromatin interactions
ENSG00000163565	chromatin interactions
ENSG00000270141	chromatin interactions

Extended variants
information (count: 402 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562881526	chr1:158961840-158961841	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78370385	chr1:158961923-158961924	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182710225	chr1:158961975-158961976	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575685991	chr1:158961982-158961983	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs57939959	chr1:158962004-158962005	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs66629384	chr1:158962005-158962006	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530287604	chr1:158962006-158962007	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs71726847	chr1:158962014-158962015	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs397732564	chr1:158962024-158962025	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs28751911	chr1:158962025-158962026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559925372	chr1:158962039-158962040	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527549444	chr1:158962084-158962085	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372485636	chr1:158962141-158962142	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs80096786	chr1:158962158-158962159	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558479973	chr1:158962169-158962170	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377242747	chr1:158962183-158962184	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140544400	chr1:158962213-158962214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77733256	chr1:158962223-158962224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12122282	chr1:158962257-158962258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115329496	chr1:158962380-158962381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559323754	chr1:158962405-158962406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111394679	chr1:158962436-158962437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555165057	chr1:158962458-158962459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572951788	chr1:158962484-158962485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567090954	chr1:158962485-158962486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545174167	chr1:158962500-158962501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201751618	chr1:158962549-158962550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188348488	chr1:158962555-158962556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs114211681	chr1:158962561-158962562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557916312	chr1:158962576-158962577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs137980805	chr1:158962595-158962596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114740408	chr1:158962613-158962614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199854251	chr1:158962647-158962648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78643366	chr1:158962650-158962651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142080898	chr1:158962656-158962657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74214257	chr1:158962663-158962664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201546969	chr1:158962682-158962683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551524110	chr1:158962708-158962709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571331482	chr1:158962722-158962723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138663514	chr1:158962725-158962726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557024394	chr1:158962744-158962745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573572236	chr1:158962749-158962750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536163702	chr1:158962750-158962751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193033306	chr1:158962762-158962763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556525266	chr1:158962767-158962768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75000900	chr1:158962774-158962775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79536632	chr1:158962812-158962813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559890258	chr1:158962847-158962848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544768696	chr1:158962871-158962872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142723086	chr1:158962901-158962902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
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
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
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
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
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158950800-158965600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:158951200-158965600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr1:158953600-158965400	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr1:158953600-158965600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr1:158954400-158968400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr1:158955000-158968200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr1:158955800-158963600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr1:158956600-158966000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr1:158957000-158965800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr1:158960600-158963200	Strong transcription	Primary T cells fromperipheralblood	blood
11	chr1:158960800-158965600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:158960800-158975400	Weak transcription	Spleen	Spleen
13	chr1:158961000-158961800	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr1:158961000-158965800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr1:158961000-158968200	Weak transcription	Primary B cells from cord blood	blood
16	chr1:158961400-158963000	Strong transcription	Primary T cells from cord blood	blood
17	chr1:158961800-158962000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
18	chr1:158961800-158962200	Enhancers	Placenta	Placenta
19	chr1:158962000-158965600	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr1:158963000-158968200	Weak transcription	Primary T cells from cord blood	blood
21	chr1:158963200-158965600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr1:158963600-158965400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr1:158964800-158965000	ZNF genes & repeats	Fetal Kidney	kidney
24	chr1:158965000-158968200	Weak transcription	Fetal Kidney	kidney
25	chr1:158965400-158966000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr1:158965400-158968800	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr1:158965600-158965800	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr1:158965600-158966800	Enhancers	Primary T cells fromperipheralblood	blood
29	chr1:158965600-158966800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr1:158965600-158968000	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr1:158965600-158969000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr1:158965600-158969000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr1:158965800-158966000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr1:158965800-158966000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
35	chr1:158965800-158966200	Enhancers	Primary B cells from peripheral blood	blood
36	chr1:158965800-158966200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr1:158965800-158968200	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr1:158965800-158968600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:158966000-158966200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
40	chr1:158966000-158966400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
41	chr1:158966000-158966600	Enhancers	GM12878-XiMat	blood
42	chr1:158966000-158966800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr1:158966000-158967200	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr1:158966200-158966600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
45	chr1:158966200-158967400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr1:158966200-158968000	Weak transcription	Primary B cells from peripheral blood	blood
47	chr1:158966400-158968000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr1:158966600-158967000	Flanking Active TSS	GM12878-XiMat	blood
49	chr1:158966600-158968600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr1:158966800-158967000	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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