Variant report

Variant	nsv542990
Chromosome Location	chr16:80729797-80918198
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1648)
CpG islands
(count:305)
Chromatin interactive
region (count:170)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:80858664-80859023	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:80862419-80862797	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:80902859-80902964	K562	blood:	n/a	n/a
4	ARID3A	chr16:80917098-80917501	HepG2	liver:	n/a	n/a
5	ATF1	chr16:80828045-80828147	K562	blood:	n/a	n/a
6	ATF1	chr16:80861785-80861816	K562	blood:	n/a	n/a
7	ATF1	chr16:80810260-80810424	K562	blood:	n/a	n/a
8	ATF2	chr16:80754470-80755094	GM12878	blood:	n/a	n/a
9	ATF2	chr16:80754391-80755239	GM12878	blood:	n/a	n/a
10	BACH1	chr16:80907272-80907341	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr16:80837137-80837466	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr16:80773513-80773713	GM12878	blood:	n/a	chr16:80773626-80773637
13	BCL3	chr16:80752900-80753077	GM12878	blood:	n/a	n/a
14	BCL3	chr16:80754467-80755188	GM12878	blood:	n/a	n/a
15	BCL3	chr16:80838415-80838640	GM12878	blood:	n/a	n/a
16	BCLAF1	chr16:80754438-80755176	GM12878	blood:	n/a	n/a
17	BCLAF1	chr16:80744616-80745186	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:80917160-80917478	HepG2	liver:	n/a	n/a
19	BHLHE40	chr16:80754676-80754876	GM12878	blood:	n/a	n/a
20	BRCA1	chr16:80869954-80870516	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr16:80880188-80881042	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr16:80837217-80837371	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr16:80868344-80868345	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr16:80870805-80872128	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr16:80878362-80878523	K562	blood:	n/a	n/a
26	CEBPB	chr16:80772341-80772898	MCF-7	breast:	n/a	chr16:80772590-80772601
27	CEBPB	chr16:80772537-80772732	K562	blood:	n/a	chr16:80772590-80772601
28	CEBPB	chr16:80917139-80917496	ECC-1	luminal epithelium:	n/a	chr16:80917279-80917288 chr16:80917279-80917290 chr16:80917277-80917288
29	CEBPB	chr16:80846654-80847307	A549	lung:	n/a	chr16:80847127-80847138
30	CEBPB	chr16:80917126-80917516	HepG2	liver:	n/a	chr16:80917279-80917288 chr16:80917279-80917290 chr16:80917277-80917288
31	CEBPB	chr16:80785016-80785433	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr16:80743564-80743629	A549	lung:	n/a	n/a
33	CEBPB	chr16:80917228-80917403	IMR90	lung:	n/a	chr16:80917279-80917288 chr16:80917279-80917290 chr16:80917277-80917288
34	CEBPB	chr16:80841842-80842194	HepG2	liver:	n/a	chr16:80842024-80842035 chr16:80841915-80841926
35	CEBPB	chr16:80772374-80772810	MCF-7	breast:	n/a	chr16:80772590-80772601
36	CEBPB	chr16:80814876-80815173	HepG2	liver:	n/a	chr16:80815044-80815055 chr16:80815044-80815053
37	CEBPB	chr16:80882500-80882752	HepG2	liver:	n/a	chr16:80882578-80882589 chr16:80882591-80882602
38	CEBPB	chr16:80772474-80772690	A549	lung:	n/a	chr16:80772590-80772601
39	CEBPB	chr16:80846525-80847204	Hela-S3	cervix:	n/a	chr16:80847127-80847138
40	CEBPB	chr16:80846534-80847311	HepG2	liver:	n/a	chr16:80847127-80847138
41	CEBPB	chr16:80752300-80752871	MCF-7	breast:	n/a	n/a
42	CEBPB	chr16:80775638-80776049	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr16:80844902-80845087	HepG2	liver:	n/a	chr16:80844963-80844974
44	CEBPB	chr16:80778803-80779015	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:80917053-80917460	MCF-7	breast:	n/a	chr16:80917279-80917288 chr16:80917279-80917290 chr16:80917277-80917288
46	CEBPB	chr16:80844912-80844953	A549	lung:	n/a	n/a
47	CEBPB	chr16:80917139-80917418	K562	blood:	n/a	chr16:80917279-80917288 chr16:80917279-80917290 chr16:80917277-80917288
48	CEBPB	chr16:80772464-80772750	Hela-S3	cervix:	n/a	chr16:80772590-80772601
49	CEBPB	chr16:80838097-80838323	IMR90	lung:	n/a	n/a
50	CEBPB	chr16:80882458-80882767	Hela-S3	cervix:	n/a	chr16:80882578-80882589 chr16:80882591-80882602

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:80838258-80838308	PFSK-1	brain:	n/a
2	chr16:80838738-80838788	HEK293	kidney:	embryo
3	chr16:80838265-80838315	AG04450	lung:	fetal
4	chr16:80838265-80838315	ProgFib	skin:	n/a
5	chr16:80839183-80839233	NHBE	bronchial:	n/a
6	chr16:80838265-80838315	GM06990	blood:	n/a
7	chr16:80839183-80839233	ProgFib	skin:	n/a
8	chr16:80839183-80839233	Caco-2	colon:	n/a
9	chr16:80838738-80838788	HAEpiC	amniotic membrane:	n/a
10	chr16:80838738-80838788	GM12878	blood:	n/a
11	chr16:80838738-80838788	GM19239	blood:	n/a
12	chr16:80838258-80838308	HPAEpiC	pulmonary alveolar:	n/a
13	chr16:80838738-80838788	ProgFib	skin:	n/a
14	chr16:80838265-80838315	BE2_C	brain:	n/a
15	chr16:80838258-80838308	CMK	blood:	n/a
16	chr16:80838738-80838788	AG10803	skin:	n/a
17	chr16:80838258-80838308	PANC-1	pancreas:	n/a
18	chr16:80839183-80839233	T-47D	breast:	n/a
19	chr16:80838265-80838315	PFSK-1	brain:	n/a
20	chr16:80824726-80824776	NHBE	bronchial:	n/a
21	chr16:80838738-80838788	GM12891	blood:	n/a
22	chr16:80839183-80839233	AG09319	gingival:	n/a
23	chr16:80824726-80824776	PANC-1	pancreas:	n/a
24	chr16:80824726-80824776	HRCEpiC	kidney:	n/a
25	chr16:80839183-80839233	MCF-7	breast:	n/a
26	chr16:80838738-80838788	A549	lung:	n/a
27	chr16:80824726-80824776	BE2_C	brain:	n/a
28	chr16:80838265-80838315	HNPCEpiC	eye:	n/a
29	chr16:80839183-80839233	HepG2	liver:	n/a
30	chr16:80824726-80824776	ProgFib	skin:	n/a
31	chr16:80839183-80839233	U87	brain:	n/a
32	chr16:80838258-80838308	ProgFib	skin:	n/a
33	chr16:80838258-80838308	H1-hESC	embryonic stem cell:	embryo
34	chr16:80824726-80824776	MCF-7	breast:	n/a
35	chr16:80838258-80838308	Caco-2	colon:	n/a
36	chr16:80838258-80838308	AG04449	skin:	fetal
37	chr16:80839183-80839233	SK-N-SH	brain:	n/a
38	chr16:80838258-80838308	HIPEpiC	eye:	n/a
39	chr16:80824726-80824776	AG09319	gingival:	n/a
40	chr16:80838265-80838315	H1-hESC	embryonic stem cell:	embryo
41	chr16:80838258-80838308	GM12892	blood:	n/a
42	chr16:80838738-80838788	HCT-116	colon:	n/a
43	chr16:80838265-80838315	SK-N-MC	brain:	n/a
44	chr16:80838265-80838315	K562	blood:	n/a
45	chr16:80839183-80839233	HIPEpiC	eye:	n/a
46	chr16:80838738-80838788	BJ	skin:	n/a
47	chr16:80824726-80824776	HIPEpiC	eye:	n/a
48	chr16:80838738-80838788	PrEC	prostate:	n/a
49	chr16:80839183-80839233	HNPCEpiC	eye:	n/a
50	chr16:80839183-80839233	HUVEC	blood vessel:	n/a

(count:170 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr16:80708985..80711337-chr16:80752928..80755974,3	MCF-7	breast:
2	chr16:80745399..80748636-chr16:80750570..80752384,3	MCF-7	breast:
3	chr16:80831187..80832847-chr16:80836382..80838874,2	MCF-7	breast:
4	chr16:80826433..80828352-chr16:80832808..80835900,4	MCF-7	breast:
5	chr16:80732152..80734988-chr16:80742943..80745813,2	MCF-7	breast:
6	chr16:80824976..80826514-chr16:80830210..80831718,2	K562	blood:
7	chr16:80823546..80825954-chr16:80836176..80839354,3	MCF-7	breast:
8	chr16:80852508..80854176-chr16:80857247..80859304,2	K562	blood:
9	chr16:80890324..80891930-chr16:80892520..80894497,2	MCF-7	breast:
10	chr16:80859688..80861227-chr16:80862399..80864225,2	MCF-7	breast:
11	chr16:80756696..80758393-chr16:80759913..80761875,2	MCF-7	breast:
12	chr16:80852508..80854176-chr16:80857247..80859304,2	K562	blood:
13	chr16:80868740..80871247-chr16:80871583..80874485,2	K562	blood:
14	chr16:80742029..80744707-chr16:80834367..80837032,2	MCF-7	breast:
15	chr16:80880174..80884302-chr16:80884623..80886773,4	MCF-7	breast:
16	chr16:80857146..80859667-chr16:80861223..80862793,2	K562	blood:
17	chr16:80715724..80718304-chr16:80740756..80743210,2	MCF-7	breast:
18	chr16:80560536..80561900-chr16:80858338..80859410,14	MCF-7	breast:
19	chr11:62608717..62609643-chr16:80871985..80872594,2	Hela-S3	cervix:
20	chr16:80752658..80755251-chr16:80863514..80866042,2	MCF-7	breast:
21	chr16:80824031..80826167-chr16:80833727..80836250,2	MCF-7	breast:
22	chr16:80795153..80796921-chr16:80801305..80802952,2	MCF-7	breast:
23	chr16:80858781..80859754-chr16:80885898..80886889,3	MCF-7	breast:
24	chr16:80836267..80838116-chr16:81067816..81069508,2	MCF-7	breast:
25	chr16:80826433..80828352-chr16:80832808..80835900,4	MCF-7	breast:
26	chr16:80829092..80831427-chr16:80833348..80835042,2	MCF-7	breast:
27	chr16:80736212..80738692-chr16:80749394..80751411,2	MCF-7	breast:
28	chr16:80857526..80859667-chr16:80861223..80862909,2	K562	blood:
29	chr16:80841190..80844369-chr16:80857041..80859496,3	MCF-7	breast:
30	chr16:80745399..80748636-chr16:80750570..80752384,3	MCF-7	breast:
31	chr16:80789011..80790811-chr16:80792089..80794243,2	MCF-7	breast:
32	chr16:80756696..80758393-chr16:80759913..80761875,2	MCF-7	breast:
33	chr16:80856381..80858777-chr16:80863162..80866586,3	K562	blood:
34	chr16:80824031..80826167-chr16:80833727..80836250,2	MCF-7	breast:
35	chr16:80809291..80811612-chr16:80817355..80819809,2	MCF-7	breast:
36	chr16:80871769..80873750-chr16:80874253..80880018,5	MCF-7	breast:
37	chr16:80841138..80843901-chr16:80845337..80848093,3	MCF-7	breast:
38	chr16:80731285..80733267-chr16:80733404..80735204,2	MCF-7	breast:
39	chr16:80897559..80901306-chr16:80907284..80910371,3	MCF-7	breast:
40	chr16:80886274..80886849-chr16:80933809..80934549,2	MCF-7	breast:
41	chr16:80779693..80781322-chr16:80792403..80794824,2	MCF-7	breast:
42	chr16:80858781..80859754-chr16:80885898..80886889,3	MCF-7	breast:
43	chr16:80826270..80828360-chr16:80833260..80835837,2	MCF-7	breast:
44	chr16:80789011..80790811-chr16:80792089..80794243,2	MCF-7	breast:
45	chr16:80650294..80652166-chr16:80871935..80873691,2	MCF-7	breast:
46	chr16:80765116..80767269-chr16:80784443..80786538,2	MCF-7	breast:
47	chr16:80859688..80861227-chr16:80862399..80864225,2	MCF-7	breast:
48	chr16:80779693..80781322-chr16:80792403..80794824,2	MCF-7	breast:
49	chr16:80723055..80725180-chr16:80728525..80730099,2	MCF-7	breast:
50	chr16:80744947..80746729-chr16:80753397..80755885,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DYNLRB2-1	chr16:80770257-80770412	ENSG00000260594.1
2	lnc-CDYL2-4	chr16:80871829-80871942	ENSG00000260896.1
3	lnc-CDYL2-4	chr16:80864323-80864654	ENSG00000260896.1
4	lnc-CDYL2-4	chr16:80874016-80874119	ENSG00000260896.1
5	lnc-DYNLRB2-1	chr16:80775995-80776202	ENSG00000260594.1
6	lnc-CDYL2-4	chr16:80864391-80864654	ENSG00000260896.1
7	lnc-CDYL2-4	chr16:80862632-80864654	ENSG00000260896.1
8	lnc-CDYL2-4	chr16:80864428-80864654	ENSG00000260896.1
9	lnc-CDYL2-4	chr16:80871829-80872402	XLOC_012021
10	lnc-CDYL2-4	chr16:80874016-80874119	ENSG00000260896.1
11	lnc-CDYL2-4	chr16:80871829-80871942	ENSG00000260896.1
12	lnc-CDYL2-4	chr16:80904345-80904417	ENSG00000260896.1
13	lnc-CDYL2-4	chr16:80862435-80864654	XLOC_012021
14	lnc-DYNLRB2-1	chr16:80772558-80772645	ENSG00000260594.1
15	lnc-CDYL2-4	chr16:80874016-80874119	ENSG00000260896.1
16	lnc-CDYL2-4	chr16:80869554-80869686	ENSG00000260896.1

No data

Variant related genes	Relation type
ENSG00000260594	TF binding region
CDYL2	TF binding region
ENSG00000260896	TF binding region
ENSG00000260594	CpG island
CDYL2	CpG island
ENSG00000260896	CpG island
ENSG00000260896	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000103363	chromatin interactions
ENSG00000260183	chromatin interactions
ENSG00000259867	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000166446	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000168589	chromatin interactions
ENSG00000196374	chromatin interactions
ENSG00000182611	chromatin interactions

Extended variants
information (count: 8396 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:8396 , 50 per page) page: 1 2 3 4 5 6 7 ... 168

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73593040	chr16:80729803-80729804	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560540149	chr16:80729807-80729808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566117196	chr16:80729815-80729816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536751405	chr16:80729836-80729837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs180917898	chr16:80729841-80729842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115567385	chr16:80729844-80729845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185791192	chr16:80729869-80729870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559172509	chr16:80729881-80729882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577491177	chr16:80729890-80729891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540976451	chr16:80729893-80729894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559095981	chr16:80729905-80729906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192361266	chr16:80729915-80729916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574137462	chr16:80729946-80729947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148765144	chr16:80729980-80729981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563071558	chr16:80730007-80730008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530602978	chr16:80730015-80730016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552101867	chr16:80730030-80730031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564375651	chr16:80730041-80730042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183752388	chr16:80730055-80730056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117514863	chr16:80730135-80730136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565923304	chr16:80730160-80730161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187289486	chr16:80730171-80730172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548689112	chr16:80730179-80730180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77698627	chr16:80730182-80730183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142477969	chr16:80730190-80730191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532360357	chr16:80730193-80730194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558890738	chr16:80730232-80730233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113427777	chr16:80730260-80730261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190778954	chr16:80730325-80730326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76411733	chr16:80730337-80730338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs59561292	chr16:80730379-80730380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574073718	chr16:80730430-80730431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140577684	chr16:80730437-80730438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556605941	chr16:80730438-80730439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149988444	chr16:80730444-80730445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545935189	chr16:80730489-80730490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564132930	chr16:80730515-80730516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528327012	chr16:80730535-80730536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540149601	chr16:80730538-80730539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75479980	chr16:80730627-80730628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79323366	chr16:80730628-80730629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561988550	chr16:80730641-80730642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9936059	chr16:80730647-80730648	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs548627813	chr16:80730651-80730652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570119849	chr16:80730656-80730657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9922837	chr16:80730657-80730658	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs146536541	chr16:80730672-80730673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369537553	chr16:80730675-80730676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75676759	chr16:80730707-80730708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76872993	chr16:80730709-80730710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Breast cancer	17603634	CNVD
Prostate cancer	16573809	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 lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1058 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80689000-80751000	Weak transcription	Pancreas	Pancrea
2	chr16:80706200-80734400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr16:80719000-80746800	Weak transcription	Spleen	Spleen
4	chr16:80725600-80734200	Weak transcription	Hela-S3	cervix
5	chr16:80727600-80732200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr16:80727800-80732400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr16:80729200-80730000	Enhancers	GM12878-XiMat	blood
8	chr16:80729200-80732800	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr16:80729400-80732400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr16:80730800-80731600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr16:80731800-80732600	Weak transcription	GM12878-XiMat	blood
12	chr16:80732200-80733000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr16:80732400-80732600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr16:80732400-80733000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr16:80732600-80732800	ZNF genes & repeats	GM12878-XiMat	blood
16	chr16:80732800-80733000	Weak transcription	GM12878-XiMat	blood
17	chr16:80733000-80734600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr16:80733000-80742600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr16:80734200-80735600	Strong transcription	Hela-S3	cervix
20	chr16:80734400-80735000	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr16:80734400-80735000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr16:80734600-80734800	Enhancers	Duodenum Mucosa	Duodenum
23	chr16:80734600-80735000	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr16:80734600-80735200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr16:80734800-80735000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr16:80734800-80736000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr16:80735000-80737200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr16:80735600-80737200	Weak transcription	Hela-S3	cervix
29	chr16:80735800-80739400	Enhancers	Fetal Intestine Small	intestine
30	chr16:80736000-80737400	Enhancers	Duodenum Mucosa	Duodenum
31	chr16:80736400-80736600	Weak transcription	Gastric	stomach
32	chr16:80736400-80738600	Enhancers	Fetal Intestine Large	intestine
33	chr16:80736600-80738400	Enhancers	Gastric	stomach
34	chr16:80737000-80737200	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr16:80737200-80737600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr16:80737200-80738200	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr16:80737200-80742000	Strong transcription	Hela-S3	cervix
38	chr16:80737400-80737600	Flanking Active TSS	Duodenum Mucosa	Duodenum
39	chr16:80737400-80737800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr16:80737400-80738200	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr16:80737400-80738400	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr16:80737400-80738800	Enhancers	Small Intestine	intestine
43	chr16:80737600-80738000	Enhancers	Duodenum Mucosa	Duodenum
44	chr16:80737800-80738000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr16:80738000-80738200	Flanking Active TSS	Duodenum Mucosa	Duodenum
46	chr16:80738200-80738400	Enhancers	Duodenum Mucosa	Duodenum
47	chr16:80738400-80738600	Flanking Active TSS	Duodenum Mucosa	Duodenum
48	chr16:80738400-80751800	Weak transcription	Gastric	stomach
49	chr16:80738600-80739200	Enhancers	Duodenum Mucosa	Duodenum
50	chr16:80739400-80746200	Weak transcription	Fetal Intestine Small	intestine

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