Variant report

Variant	nsv1859
Chromosome Location	chr16:71166087-71186630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:115)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:115 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:71184717-71184907	K562	blood:	n/a	n/a
2	BACH1	chr16:71184315-71184498	K562	blood:	n/a	n/a
3	BACH1	chr16:71173649-71173792	K562	blood:	n/a	n/a
4	CBX3	chr16:71173762-71174069	K562	blood:	n/a	n/a
5	CEBPB	chr16:71173115-71173415	HepG2	liver:	n/a	chr16:71173253-71173264
6	CEBPB	chr16:71181146-71181247	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr16:71173101-71173388	Hela-S3	cervix:	n/a	chr16:71173253-71173264
8	CEBPB	chr16:71173124-71173419	IMR90	lung:	n/a	chr16:71173253-71173264
9	CEBPB	chr16:71173158-71173381	K562	blood:	n/a	chr16:71173253-71173264
10	CHD1	chr16:71176955-71177073	GM12878	blood:	n/a	n/a
11	CHD1	chr16:71178839-71178983	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr16:71176921-71176957	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr16:71177092-71177122	Fibrobl	skin:	n/a	n/a
14	CTCF	chr16:71184920-71185070	GM12872	blood:	n/a	n/a
15	CTCF	chr16:71170940-71171090	HCM	heart:	n/a	n/a
16	CTCF	chr16:71168240-71168390	GM12873	blood:	n/a	n/a
17	CTCF	chr16:71185420-71185570	GM12867	blood:	n/a	n/a
18	CUX1	chr16:71171077-71171250	K562	blood:	n/a	n/a
19	CUX1	chr16:71172285-71172289	GM12878	blood:	n/a	n/a
20	E2F4	chr16:71173446-71174368	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr16:71179447-71180539	MCF10A-Er-Src	breast:	n/a	n/a
22	ELK1	chr16:71169064-71169068	GM12878	blood:	n/a	n/a
23	ELK1	chr16:71175906-71176070	GM12878	blood:	n/a	n/a
24	ELK1	chr16:71169420-71169448	Hela-S3	cervix:	n/a	n/a
25	ELK1	chr16:71166648-71166664	GM12878	blood:	n/a	n/a
26	EP300	chr16:71174430-71174695	K562	blood:	n/a	n/a
27	EP300	chr16:71168413-71168431	HepG2	liver:	n/a	n/a
28	EP300	chr16:71171271-71171376	K562	blood:	n/a	n/a
29	EP300	chr16:71177442-71177479	GM12878	blood:	n/a	n/a
30	EP300	chr16:71177941-71178198	GM12878	blood:	n/a	chr16:71178090-71178104 chr16:71178082-71178096 chr16:71178084-71178098
31	FAM48A	chr16:71168458-71168506	GM12878	blood:	n/a	n/a
32	FAM48A	chr16:71177629-71177797	GM12878	blood:	n/a	n/a
33	FAM48A	chr16:71178390-71178443	GM12878	blood:	n/a	n/a
34	FAM48A	chr16:71172027-71172227	GM12878	blood:	n/a	n/a
35	FAM48A	chr16:71177082-71177319	GM12878	blood:	n/a	n/a
36	FOS	chr16:71175684-71175899	HUVEC	blood vessel:	n/a	n/a
37	GATA1	chr16:71173594-71174117	PBDEFetal	blood:	n/a	n/a
38	GATA3	chr16:71184288-71184759	MCF-7	breast:	n/a	n/a
39	GATA3	chr16:71170769-71171333	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr16:71180736-71181173	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr16:71174087-71174736	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr16:71176836-71177473	MCF-7	breast:	n/a	chr16:71177335-71177342 chr16:71177331-71177347
43	GATA3	chr16:71176654-71177156	SH-SY5Y	brain:	n/a	chr16:71176761-71176769
44	GATA3	chr16:71178182-71178805	SH-SY5Y	brain:	n/a	chr16:71178491-71178501
45	GATA3	chr16:71175681-71176069	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr16:71168819-71170167	SH-SY5Y	brain:	n/a	chr16:71169176-71169184 chr16:71169173-71169186
47	GATA3	chr16:71181949-71182307	SH-SY5Y	brain:	n/a	n/a
48	GTF2F1	chr16:71170806-71170887	H1-hESC	embryonic stem cell:	n/a	n/a
49	GTF2F1	chr16:71173796-71173814	H1-hESC	embryonic stem cell:	n/a	n/a
50	IKZF1	chr16:71184680-71185019	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:71168874-71168924	AoSMC	blood vessel:	n/a
2	chr16:71168874-71168924	HCT-116	colon:	n/a
3	chr16:71168874-71168924	HMEC	breast:	n/a
4	chr16:71168874-71168924	ovcar-3	ovarian:	n/a
5	chr16:71168874-71168924	GM19239	blood:	n/a
6	chr16:71168874-71168924	AG09319	gingival:	n/a
7	chr16:71168874-71168924	Hepatocyte	liver:	n/a
8	chr16:71168874-71168924	Caco-2	colon:	n/a
9	chr16:71168874-71168924	A549	lung:	n/a
10	chr16:71168874-71168924	HPAEpiC	pulmonary alveolar:	n/a
11	chr16:71168874-71168924	Jurkat	blood:	n/a
12	chr16:71168874-71168924	AG04450	lung:	fetal
13	chr16:71168874-71168924	HCM	heart:	n/a
14	chr16:71168874-71168924	NH-A	brain:	n/a
15	chr16:71168874-71168924	T-47D	breast:	n/a
16	chr16:71168874-71168924	HRCEpiC	kidney:	n/a
17	chr16:71168874-71168924	SK-N-MC	brain:	n/a
18	chr16:71168874-71168924	SK-N-SH	brain:	n/a
19	chr16:71168874-71168924	BJ	skin:	n/a
20	chr16:71168874-71168924	ECC-1	luminal epithelium:	n/a
21	chr16:71168874-71168924	K562	blood:	n/a
22	chr16:71168874-71168924	GM12892	blood:	n/a
23	chr16:71168874-71168924	SAEC	small airway:	n/a
24	chr16:71168874-71168924	MCF-7	breast:	n/a
25	chr16:71168874-71168924	HAEpiC	amniotic membrane:	n/a
26	chr16:71168874-71168924	GM12891	blood:	n/a
27	chr16:71168874-71168924	Hela-S3	cervix:	n/a
28	chr16:71168874-71168924	GM12878	blood:	n/a
29	chr16:71168874-71168924	HRE	kidney:	n/a
30	chr16:71168874-71168924	NT2-D1	testis:	n/a
31	chr16:71168874-71168924	BE2_C	brain:	n/a
32	chr16:71168874-71168924	HRPEpiC	eye:	n/a
33	chr16:71168874-71168924	MCF10A-Er-Src	breast:	n/a
34	chr16:71168874-71168924	HNPCEpiC	eye:	n/a
35	chr16:71168874-71168924	HIPEpiC	eye:	n/a
36	chr16:71168874-71168924	HEEpiC	esophagus:	n/a
37	chr16:71168874-71168924	SKMC	muscle:	n/a
38	chr16:71168874-71168924	ProgFib	skin:	n/a
39	chr16:71168874-71168924	PFSK-1	brain:	n/a
40	chr16:71168874-71168924	LNCaP	prostate:	n/a
41	chr16:71168874-71168924	SK-N-SH_RA	brain:	n/a
42	chr16:71168874-71168924	HEK293	kidney:	embryo
43	chr16:71168874-71168924	CMK	blood:	n/a
44	chr16:71168874-71168924	PrEC	prostate:	n/a
45	chr16:71168874-71168924	AG10803	skin:	n/a
46	chr16:71168874-71168924	HCPEpiC	choroid plexus:	n/a
47	chr16:71168874-71168924	NHBE	bronchial:	n/a
48	chr16:71168874-71168924	HUVEC	blood vessel:	n/a
49	chr16:71168874-71168924	GM06990	blood:	n/a
50	chr16:71168874-71168924	HL-60	blood:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:71158993..71163306-chr16:71165421..71171777,6	MCF-7	breast:
2	chr16:71173614..71175656-chr16:71176168..71177672,2	K562	blood:
3	chr16:71164439..71166621-chr16:71171910..71174347,2	MCF-7	breast:
4	chr1:146554737..146556264-chr16:71167039..71168689,2	K562	blood:
5	chr16:71169222..71171433-chr16:71173024..71177252,4	K562	blood:
6	chr16:71161791..71164496-chr16:71177247..71181624,3	K562	blood:
7	chr16:71127059..71128576-chr16:71174423..71176284,2	MCF-7	breast:
8	chr16:71177450..71180363-chr16:71183584..71186002,2	K562	blood:
9	chr16:71169999..71172997-chr16:71175859..71177965,3	MCF-7	breast:
10	chr16:71180800..71183455-chr16:71191857..71194078,2	K562	blood:
11	chr16:71164439..71166621-chr16:71171910..71174347,2	MCF-7	breast:
12	chr16:71176614..71178323-chr16:71181138..71183405,2	K562	blood:
13	chr16:71161173..71163942-chr16:71164810..71166980,2	MCF-7	breast:
14	chr16:71176614..71178323-chr16:71181138..71183405,2	K562	blood:
15	chr16:71173614..71175656-chr16:71176168..71177672,2	K562	blood:
16	chr16:71177483..71180082-chr16:71181672..71184135,2	MCF-7	breast:
17	chr16:71184127..71186563-chr16:71187972..71191511,3	MCF-7	breast:
18	chr16:71177239..71178850-chr16:71198965..71201632,2	K562	blood:
19	chr16:71169222..71171433-chr16:71173024..71177252,4	K562	blood:
20	chr16:71174258..71176260-chr16:71176736..71179673,2	MCF-7	breast:
21	chr16:71177483..71180082-chr16:71181672..71184135,2	MCF-7	breast:
22	chr16:71174258..71176260-chr16:71176736..71179673,2	MCF-7	breast:
23	chr16:71177450..71182290-chr16:71183584..71187452,4	K562	blood:
24	chr16:71169999..71172997-chr16:71175859..71177965,3	MCF-7	breast:
25	chr16:71153149..71155855-chr16:71181405..71183905,2	K562	blood:
26	chr16:71164216..71166696-chr16:71169224..71171116,2	K562	blood:
27	chr16:71164216..71166696-chr16:71169224..71171116,2	K562	blood:
28	chr16:71177450..71180363-chr16:71183584..71186002,2	K562	blood:

No data

Variant related genes	Relation type
HYDIN	TF binding region
HYDIN	CpG island
ENSG00000230832	chromatin interactions
ENSG00000157423	chromatin interactions

Extended variants
information (count: 682 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:682 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11075875	chr16:71166188-71166189	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs113791718	chr16:71166285-71166286	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs577828006	chr16:71166286-71166287	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs11075876	chr16:71166338-71166339	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11075877	chr16:71166386-71166387	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs57087173	chr16:71166402-71166403	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563854476	chr16:71166541-71166542	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs16964541	chr16:71166556-71166557	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs200527318	chr16:71166575-71166576	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs9936905	chr16:71166631-71166632	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs148679146	chr16:71166635-71166636	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs372469493	chr16:71166639-71166640	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs141258671	chr16:71166640-71166641	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201996009	chr16:71166641-71166642	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs199542328	chr16:71166643-71166644	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs560887189	chr16:71166653-71166654	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs11647627	chr16:71166771-71166772	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs372550426	chr16:71166788-71166789	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201018234	chr16:71166807-71166808	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs546726254	chr16:71166832-71166833	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs150763207	chr16:71166862-71166863	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs201854236	chr16:71166864-71166865	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs554073181	chr16:71166865-71166866	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs113586766	chr16:71166870-71166871	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs538502812	chr16:71166920-71166921	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550831769	chr16:71166986-71166987	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs979208	chr16:71167013-71167014	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs536563398	chr16:71167014-71167015	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs7500756	chr16:71167036-71167037	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113069766	chr16:71167053-71167054	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs555447776	chr16:71167147-71167148	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs2040830	chr16:71167220-71167221	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs573704128	chr16:71167265-71167266	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534756744	chr16:71167315-71167316	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs111447746	chr16:71167334-71167335	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553094370	chr16:71167346-71167347	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs979209	chr16:71167349-71167350	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs577815507	chr16:71167360-71167361	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs184197560	chr16:71167365-71167366	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs187514534	chr16:71167382-71167383	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372181560	chr16:71167407-71167408	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs575818133	chr16:71167408-71167409	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs543305929	chr16:71167427-71167428	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs58545356	chr16:71167466-71167467	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11075878	chr16:71167501-71167502	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs560826268	chr16:71167518-71167519	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs61406144	chr16:71167546-71167547	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs369988029	chr16:71167550-71167551	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2040831	chr16:71167564-71167565	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs528133534	chr16:71167632-71167633	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	18923524	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71148800-71172200	Weak transcription	Fetal Brain Male	brain
2	chr16:71151400-71168600	Weak transcription	Fetal Lung	lung
3	chr16:71158400-71191600	Weak transcription	Fetal Intestine Small	intestine
4	chr16:71159000-71171200	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr16:71160600-71185200	Weak transcription	Pancreas	Pancrea
6	chr16:71162000-71169200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr16:71162400-71169600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr16:71162600-71168200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr16:71162600-71168400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr16:71162800-71168600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr16:71163200-71169000	Weak transcription	Stomach Smooth Muscle	stomach
12	chr16:71163200-71169800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr16:71163200-71172600	Weak transcription	Fetal Intestine Large	intestine
14	chr16:71163200-71191600	Weak transcription	Fetal Stomach	stomach
15	chr16:71163400-71166600	Weak transcription	Brain Germinal Matrix	brain
16	chr16:71163400-71166600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr16:71163600-71166200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr16:71163600-71166400	Weak transcription	Brain Anterior Caudate	brain
19	chr16:71163600-71166800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr16:71163600-71168200	Weak transcription	Brain Hippocampus Middle	brain
21	chr16:71163600-71168400	Weak transcription	Brain Substantia Nigra	brain
22	chr16:71163600-71172400	Weak transcription	Fetal Kidney	kidney
23	chr16:71163600-71173600	Weak transcription	Brain Angular Gyrus	brain
24	chr16:71163600-71173800	Weak transcription	Brain Cingulate Gyrus	brain
25	chr16:71163800-71168400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr16:71164000-71168400	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr16:71164000-71170800	Weak transcription	Dnd41	blood
28	chr16:71164200-71168600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr16:71165000-71169400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr16:71165400-71166400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr16:71165600-71168600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr16:71166000-71168600	ZNF genes & repeats	Aorta	Aorta
33	chr16:71166000-71168800	Strong transcription	Fetal Brain Female	brain
34	chr16:71166200-71167000	Strong transcription	Duodenum Smooth Muscle	Duodenum
35	chr16:71166400-71166800	Strong transcription	Brain Anterior Caudate	brain
36	chr16:71166400-71167400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr16:71166600-71167000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
38	chr16:71166600-71168000	Enhancers	Brain Germinal Matrix	brain
39	chr16:71166800-71167200	Strong transcription	Brain Inferior Temporal Lobe	brain
40	chr16:71166800-71167600	Genic enhancers	Brain Anterior Caudate	brain
41	chr16:71167000-71167600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr16:71167000-71169000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr16:71167000-71173200	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr16:71167200-71170800	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr16:71167400-71168600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr16:71167600-71169800	Enhancers	Brain Anterior Caudate	brain
47	chr16:71168000-71168600	Genic enhancers	Brain Germinal Matrix	brain
48	chr16:71168000-71168800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr16:71168000-71169800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr16:71168000-71170000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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