Variant report

Variant	nsv873210
Chromosome Location	chr1:223707647-223856414
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1187)
CpG islands
(count:1101)
Chromatin interactive
region (count:57)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1187 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:223803124-223803125	K562	blood:	n/a	n/a
2	ATF1	chr1:223803986-223804103	K562	blood:	n/a	n/a
3	ATF2	chr1:223720936-223721318	GM12878	blood:	n/a	n/a
4	ATF3	chr1:223816000-223816218	K562	blood:	n/a	n/a
5	ATF3	chr1:223855311-223855575	K562	blood:	n/a	n/a
6	BACH1	chr1:223834947-223834971	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr1:223819895-223820243	GM12878	blood:	n/a	n/a
8	BATF	chr1:223809024-223809509	GM12878	blood:	n/a	n/a
9	BATF	chr1:223808049-223808372	GM12878	blood:	n/a	chr1:223808205-223808216
10	BATF	chr1:223720933-223721309	GM12878	blood:	n/a	n/a
11	BATF	chr1:223809028-223809426	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:223720942-223721314	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:223809058-223809350	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:223808999-223809391	GM12878	blood:	n/a	n/a
15	BCL3	chr1:223720885-223721302	GM12878	blood:	n/a	n/a
16	BCL3	chr1:223809039-223809430	GM12878	blood:	n/a	n/a
17	BCL3	chr1:223842759-223843334	A549	lung:	n/a	n/a
18	BHLHE40	chr1:223815889-223816261	K562	blood:	n/a	n/a
19	BHLHE40	chr1:223725113-223725463	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:223720800-223721279	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:223709492-223709560	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:223809040-223809519	GM12878	blood:	n/a	n/a
23	CBX3	chr1:223815860-223816359	K562	blood:	n/a	n/a
24	CBX3	chr1:223731744-223732129	K562	blood:	n/a	n/a
25	CEBPB	chr1:223851734-223852179	MCF-7	breast:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
26	CEBPB	chr1:223826848-223827494	MCF-7	breast:	n/a	chr1:223827097-223827108
27	CEBPB	chr1:223855372-223855554	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:223851716-223852214	MCF-7	breast:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
29	CEBPB	chr1:223851815-223852192	K562	blood:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
30	CEBPB	chr1:223851813-223852188	HepG2	liver:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
31	CEBPB	chr1:223825571-223825761	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:223851676-223852259	A549	lung:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
33	CEBPB	chr1:223826960-223827254	A549	lung:	n/a	chr1:223827097-223827108
34	CEBPB	chr1:223835053-223835253	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr1:223844841-223844933	HepG2	liver:	n/a	chr1:223844867-223844880 chr1:223844866-223844883 chr1:223844867-223844880
36	CEBPB	chr1:223851818-223852190	A549	lung:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
37	CEBPB	chr1:223822220-223822370	HepG2	liver:	n/a	n/a
38	CEBPB	chr1:223842598-223843268	MCF-7	breast:	n/a	n/a
39	CEBPB	chr1:223851859-223852168	H1-hESC	embryonic stem cell:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
40	CEBPB	chr1:223851845-223852146	ECC-1	luminal epithelium:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
41	CEBPB	chr1:223826932-223827280	Hela-S3	cervix:	n/a	chr1:223827097-223827108
42	CEBPB	chr1:223840146-223840530	MCF-7	breast:	n/a	n/a
43	CEBPB	chr1:223851821-223852161	K562	blood:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
44	CEBPB	chr1:223851823-223852172	IMR90	lung:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
45	CEBPB	chr1:223826966-223827207	HepG2	liver:	n/a	chr1:223827097-223827108
46	CEBPB	chr1:223826953-223827268	K562	blood:	n/a	chr1:223827097-223827108
47	CEBPB	chr1:223851839-223852173	Hela-S3	cervix:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
48	CEBPB	chr1:223826952-223827252	K562	blood:	n/a	chr1:223827097-223827108
49	CEBPB	chr1:223812732-223812865	K562	blood:	n/a	n/a
50	CEBPB	chr1:223851866-223852042	HepG2	liver:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:223743086-223743136	GM12891	blood:	n/a
2	chr1:223740057-223740107	GM06990	blood:	n/a
3	chr1:223854639-223854689	GM12891	blood:	n/a
4	chr1:223743086-223743136	GM12891	blood:	n/a
5	chr1:223740057-223740107	GM06990	blood:	n/a
6	chr1:223854639-223854689	GM12891	blood:	n/a
7	chr1:223747670-223747720	Hepatocyte	liver:	n/a
8	chr1:223854639-223854689	MCF10A-Er-Src	breast:	n/a
9	chr1:223854704-223854754	RPTEC	kidney:	n/a
10	chr1:223835369-223835419	RPTEC	kidney:	n/a
11	chr1:223853928-223853978	HEEpiC	esophagus:	n/a
12	chr1:223738388-223738438	NH-A	brain:	n/a
13	chr1:223745234-223745284	ProgFib	skin:	n/a
14	chr1:223840974-223841024	AG04449	skin:	fetal
15	chr1:223743086-223743136	BJ	skin:	n/a
16	chr1:223853928-223853978	BJ	skin:	n/a
17	chr1:223715195-223715245	HRE	kidney:	n/a
18	chr1:223854447-223854497	GM12891	blood:	n/a
19	chr1:223854639-223854689	HepG2	liver:	n/a
20	chr1:223745234-223745284	K562	blood:	n/a
21	chr1:223747670-223747720	NHDF-neo	bronchial:	n/a
22	chr1:223740057-223740107	AG09309	skin:	n/a
23	chr1:223854704-223854754	HCT-116	colon:	n/a
24	chr1:223853949-223853999	H1-hESC	embryonic stem cell:	embryo
25	chr1:223853928-223853978	HCPEpiC	choroid plexus:	n/a
26	chr1:223854639-223854689	BE2_C	brain:	n/a
27	chr1:223745234-223745284	MCF10A-Er-Src	breast:	n/a
28	chr1:223840974-223841024	AG09309	skin:	n/a
29	chr1:223853928-223853978	Jurkat	blood:	n/a
30	chr1:223835369-223835419	NB4	blood:	n/a
31	chr1:223840925-223840975	NB4	blood:	n/a
32	chr1:223853949-223853999	AG04450	lung:	fetal
33	chr1:223854639-223854689	Hepatocyte	liver:	n/a
34	chr1:223743126-223743176	PrEC	prostate:	n/a
35	chr1:223739441-223739491	MCF-7	breast:	n/a
36	chr1:223840925-223840975	SK-N-SH_RA	brain:	n/a
37	chr1:223854447-223854497	PrEC	prostate:	n/a
38	chr1:223739441-223739491	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:223741444-223741494	GM12878	blood:	n/a
40	chr1:223740057-223740107	NB4	blood:	n/a
41	chr1:223743126-223743176	AG09319	gingival:	n/a
42	chr1:223741444-223741494	Caco-2	colon:	n/a
43	chr1:223738388-223738438	ECC-1	luminal epithelium:	n/a
44	chr1:223854447-223854497	BE2_C	brain:	n/a
45	chr1:223745234-223745284	HRCEpiC	kidney:	n/a
46	chr1:223745234-223745284	AG10803	skin:	n/a
47	chr1:223835369-223835419	AoSMC	blood vessel:	n/a
48	chr1:223854639-223854689	ProgFib	skin:	n/a
49	chr1:223854639-223854689	NB4	blood:	n/a
50	chr1:223715195-223715245	ECC-1	luminal epithelium:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:223838928..223839586-chr1:223857876..223858715,2	MCF-7	breast:
2	chr1:223743774..223745290-chr9:138980904..138982846,2	MCF-7	breast:
3	chr1:223837812..223840547-chr1:223845364..223849589,4	K562	blood:
4	chr1:223831879..223834743-chr1:223845715..223848312,2	K562	blood:
5	chr1:223827148..223829506-chr1:223840054..223841666,2	MCF-7	breast:
6	chr1:223801253..223805310-chr1:223810350..223813712,3	K562	blood:
7	chr1:223809178..223812919-chr1:223814445..223817998,4	K562	blood:
8	chr1:223836208..223847031-chr1:223849408..223858826,22	MCF-7	breast:
9	chr1:223819090..223819750-chr1:223857938..223858740,2	MCF-7	breast:
10	chr1:223850712..223853354-chr1:223854192..223856571,2	MCF-7	breast:
11	chr1:223831956..223833970-chr1:223853050..223855835,2	MCF-7	breast:
12	chr1:223834427..223836360-chr1:223837595..223841642,3	MCF-7	breast:
13	chr1:223829687..223833751-chr1:223837016..223839699,4	MCF-7	breast:
14	chr1:223598585..223601286-chr1:223707386..223708910,2	MCF-7	breast:
15	chr1:223843142..223845522-chr1:223848017..223849601,2	K562	blood:
16	chr1:223833055..223835891-chr1:223854048..223855966,2	K562	blood:
17	chr1:223832588..223834103-chr1:223850844..223852665,2	MCF-7	breast:
18	chr1:223827325..223830055-chr1:223836590..223838294,2	MCF-7	breast:
19	chr1:223809528..223812099-chr1:223812404..223815945,3	K562	blood:
20	chr1:223827325..223830055-chr1:223836590..223838294,2	MCF-7	breast:
21	chr1:223846868..223849308-chr1:223851212..223853858,2	K562	blood:
22	chr1:223809528..223812099-chr1:223812404..223815945,3	K562	blood:
23	chr1:223802950..223805657-chr20:60696653..60698417,2	MCF-7	breast:
24	chr1:223825136..223827090-chr1:223853987..223856973,2	MCF-7	breast:
25	chr1:223703768..223706532-chr1:223713355..223715908,3	MCF-7	breast:
26	chr1:223823766..223826400-chr1:223828935..223830773,2	K562	blood:
27	chr1:223815744..223818238-chr1:223828274..223830462,2	K562	blood:
28	chr1:223837812..223840547-chr1:223845364..223849589,4	K562	blood:
29	chr1:223840282..223843675-chr1:223851675..223856291,7	MCF-7	breast:
30	chr1:223817010..223818658-chr1:223819579..223821945,2	K562	blood:
31	chr1:223801253..223805310-chr1:223810350..223813712,3	K562	blood:
32	chr1:223827183..223829380-chr1:223830891..223832610,2	MCF-7	breast:
33	chr1:223826154..223828830-chr1:223841356..223843010,2	MCF-7	breast:
34	chr1:223827148..223829506-chr1:223840054..223841666,2	MCF-7	breast:
35	chr1:223846678..223849774-chr1:223851871..223853598,3	MCF-7	breast:
36	chr1:223823766..223826400-chr1:223828935..223830773,2	K562	blood:
37	chr1:223832588..223834103-chr1:223850844..223852665,2	MCF-7	breast:
38	chr1:223840874..223841758-chr8:63546888..63547676,2	MCF-7	breast:
39	chr1:223817010..223818658-chr1:223819579..223821945,2	K562	blood:
40	chr1:223843142..223845522-chr1:223848017..223849601,2	K562	blood:
41	chr1:223853852..223855706-chr1:223946715..223948642,2	K562	blood:
42	chr1:223722935..223725716-chr1:223807910..223810771,2	MCF-7	breast:
43	chr1:223803243..223805245-chr1:223838331..223840277,2	MCF-7	breast:
44	chr1:223322225..223323066-chr1:223842691..223843630,2	MCF-7	breast:
45	chr1:223834427..223836360-chr1:223837595..223841642,3	MCF-7	breast:
46	chr1:223833118..223836523-chr1:223838327..223841763,4	MCF-7	breast:
47	chr1:223825136..223827090-chr1:223853987..223856973,2	MCF-7	breast:
48	chr1:223840282..223843675-chr1:223851675..223856291,7	MCF-7	breast:
49	chr1:223833055..223835891-chr1:223854048..223855966,2	K562	blood:
50	chr1:223842591..223843487-chr1:223870928..223871712,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAPN2-4	chr1:223734823-223735425	l_200_chr1:223730152-223735425_prostate
2	lnc-C1orf65-1	chr1:223726188-223726675	l_199_chr1:223725457-223726675_prostate
3	lnc-TP53BP2-5	chr1:223831812-223832085	NONHSAT009740
4	lnc-C1orf65-1	chr1:223725458-223725845	l_199_chr1:223725457-223726675_prostate
5	lnc-CAPN8-1	chr1:223719548-223719608	NONHSAT009739
6	lnc-CAPN8-1	chr1:223719548-223719668	NONHSAT009738
7	lnc-CAPN2-4	chr1:223730153-223730935	l_200_chr1:223730152-223735425_prostate

No data

Variant related genes	Relation type
ENSG00000235428	TF binding region
SNRPEP10	TF binding region
CAPN8	TF binding region
ENSG00000235428	CpG island
SNRPEP10	CpG island
CAPN8	CpG island
ENSG00000143502	chromatin interactions
ENSG00000162909	chromatin interactions
ENSG00000203697	chromatin interactions
ENSG00000149657	chromatin interactions
ENSG00000227002	chromatin interactions

Extended variants
information (count: 3460 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3460 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12123913	chr1:223707647-223707648	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183239451	chr1:223707662-223707663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187561344	chr1:223707708-223707709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192812169	chr1:223707759-223707760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560379012	chr1:223707773-223707774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs151219470	chr1:223707815-223707816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529058513	chr1:223707855-223707856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370436729	chr1:223707872-223707873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543960708	chr1:223707913-223707914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562482454	chr1:223707933-223707934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572105491	chr1:223707945-223707946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs56389919	chr1:223707954-223707955	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs74148048	chr1:223707955-223707956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs113777344	chr1:223707985-223707986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76588192	chr1:223707997-223707998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188410852	chr1:223708007-223708008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546846628	chr1:223708012-223708013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567320953	chr1:223708101-223708102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561140276	chr1:223708112-223708113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76318677	chr1:223708118-223708119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192742097	chr1:223708146-223708147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150343937	chr1:223708148-223708149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538951038	chr1:223708217-223708218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75356225	chr1:223708243-223708244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28563106	chr1:223708254-223708255	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs536602843	chr1:223708260-223708261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527687999	chr1:223708264-223708265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554654126	chr1:223708285-223708286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141278954	chr1:223708287-223708288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184051740	chr1:223708305-223708306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116717204	chr1:223708306-223708307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543766895	chr1:223708364-223708365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577903448	chr1:223708394-223708395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544987204	chr1:223708419-223708420	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560365010	chr1:223708425-223708426	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527289268	chr1:223708460-223708461	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548956248	chr1:223708482-223708483	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373069583	chr1:223708498-223708499	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145065646	chr1:223708504-223708505	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531415048	chr1:223708519-223708520	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550434425	chr1:223708547-223708548	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571763212	chr1:223708573-223708574	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570170475	chr1:223708641-223708642	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28970342	chr1:223708644-223708645	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547778881	chr1:223708666-223708667	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563270464	chr1:223708676-223708677	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372869207	chr1:223708682-223708683	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532171109	chr1:223708772-223708773	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114471471	chr1:223708773-223708774	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74932960	chr1:223708807-223708808	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Acute lymphoblastic leukemia	21098271	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
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	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
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223706200-223717800	Weak transcription	Stomach Mucosa	stomach
2	chr1:223708200-223709000	Enhancers	Skeletal Muscle Male	skeletal muscle
3	chr1:223708400-223708800	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr1:223708400-223709600	Bivalent Enhancer	Fetal Muscle Leg	muscle
5	chr1:223708400-223709800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr1:223708600-223709200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:223709000-223709200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr1:223710400-223718600	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr1:223710800-223723400	Weak transcription	Colonic Mucosa	Colon
10	chr1:223711000-223718200	Weak transcription	Gastric	stomach
11	chr1:223712000-223713400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr1:223712200-223712400	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
13	chr1:223712200-223712600	Enhancers	Brain Hippocampus Middle	brain
14	chr1:223712200-223712800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr1:223712200-223712800	Bivalent Enhancer	Fetal Muscle Leg	muscle
16	chr1:223712200-223718400	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr1:223712400-223712600	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr1:223712400-223712600	Bivalent Enhancer	Fetal Stomach	stomach
19	chr1:223712400-223712600	ZNF genes & repeats	Lung	lung
20	chr1:223712600-223713400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:223712600-223714000	Weak transcription	Lung	lung
22	chr1:223713000-223713400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr1:223713000-223716200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr1:223713200-223713800	Enhancers	Brain Substantia Nigra	brain
25	chr1:223713400-223713600	Enhancers	Brain Cingulate Gyrus	brain
26	chr1:223714000-223714200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:223714000-223714200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr1:223714000-223714400	Enhancers	Pancreas	Pancrea
29	chr1:223714400-223728200	Weak transcription	Fetal Stomach	stomach
30	chr1:223715000-223716200	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr1:223716000-223716400	Enhancers	Duodenum Mucosa	Duodenum
32	chr1:223716200-223716400	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr1:223716400-223716600	Enhancers	Small Intestine	intestine
34	chr1:223716400-223717200	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr1:223716400-223717600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr1:223717000-223717400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr1:223717600-223718800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr1:223717800-223719400	Enhancers	Stomach Mucosa	stomach
39	chr1:223718200-223718600	Enhancers	Gastric	stomach
40	chr1:223718400-223719200	Enhancers	Duodenum Mucosa	Duodenum
41	chr1:223718400-223719200	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr1:223718600-223718800	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr1:223718600-223727000	Weak transcription	Gastric	stomach
44	chr1:223718800-223723400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr1:223719200-223723400	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr1:223719400-223719800	Weak transcription	Stomach Mucosa	stomach
47	chr1:223719800-223720400	Enhancers	Stomach Mucosa	stomach
48	chr1:223720400-223723400	Weak transcription	Stomach Mucosa	stomach
49	chr1:223721400-223721800	ZNF genes & repeats	Esophagus	oesophagus
50	chr1:223721800-223723600	Weak transcription	Esophagus	oesophagus

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