Variant report

Variant	nsv561579
Chromosome Location	chr13:46154749-46208065
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	ATF1	chr13:46172103-46172395	K562	blood:	n/a	n/a
2	BACH1	chr13:46189680-46190065	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:46196280-46196441	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr13:46201201-46201466	GM12878	blood:	n/a	chr13:46201321-46201332 chr13:46201322-46201332 chr13:46201326-46201336
5	BRCA1	chr13:46189597-46189955	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr13:46182150-46182443	A549	lung:	n/a	chr13:46182268-46182279
7	CEBPB	chr13:46171257-46171599	K562	blood:	n/a	chr13:46171423-46171436 chr13:46171423-46171434 chr13:46171423-46171436 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171436 chr13:46171425-46171434
8	CEBPB	chr13:46171302-46171556	Hela-S3	cervix:	n/a	chr13:46171423-46171436 chr13:46171423-46171434 chr13:46171423-46171436 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171436 chr13:46171425-46171434
9	CEBPB	chr13:46166191-46166475	IMR90	lung:	n/a	chr13:46166310-46166321 chr13:46166309-46166322 chr13:46166309-46166320
10	CEBPB	chr13:46166177-46166436	A549	lung:	n/a	chr13:46166310-46166321 chr13:46166309-46166322 chr13:46166309-46166320
11	CEBPB	chr13:46171375-46171574	H1-hESC	embryonic stem cell:	n/a	chr13:46171423-46171436 chr13:46171423-46171434 chr13:46171423-46171436 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171436 chr13:46171425-46171434
12	CEBPB	chr13:46182104-46182370	K562	blood:	n/a	chr13:46182268-46182279
13	CEBPB	chr13:46162003-46162273	HepG2	liver:	n/a	n/a
14	CEBPB	chr13:46183870-46184037	A549	lung:	n/a	n/a
15	CEBPB	chr13:46185134-46185232	HepG2	liver:	n/a	chr13:46185177-46185188 chr13:46185176-46185189
16	CEBPB	chr13:46171250-46171596	HepG2	liver:	n/a	chr13:46171423-46171436 chr13:46171423-46171434 chr13:46171423-46171436 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171436 chr13:46171425-46171434
17	CEBPB	chr13:46182078-46182458	MCF-7	breast:	n/a	chr13:46182268-46182279
18	CEBPB	chr13:46166180-46166483	HepG2	liver:	n/a	chr13:46166310-46166321 chr13:46166309-46166322 chr13:46166309-46166320
19	CEBPB	chr13:46171270-46171607	A549	lung:	n/a	chr13:46171423-46171436 chr13:46171423-46171434 chr13:46171423-46171436 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171436 chr13:46171425-46171434
20	CEBPB	chr13:46162144-46162200	K562	blood:	n/a	n/a
21	CEBPB	chr13:46182104-46182434	HepG2	liver:	n/a	chr13:46182268-46182279
22	CEBPB	chr13:46182126-46182387	Hela-S3	cervix:	n/a	chr13:46182268-46182279
23	CEBPB	chr13:46182125-46182425	IMR90	lung:	n/a	chr13:46182268-46182279
24	CEBPB	chr13:46171253-46171613	IMR90	lung:	n/a	chr13:46171423-46171436 chr13:46171423-46171434 chr13:46171423-46171436 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171434 chr13:46171425-46171436 chr13:46171425-46171434
25	CHD1	chr13:46196509-46196563	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr13:46189592-46190094	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr13:46196362-46196450	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr13:46159040-46159190	HEEpiC	esophagus:	n/a	chr13:46159145-46159163 chr13:46159140-46159161
29	CTCF	chr13:46197740-46197890	AG04450	lung:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
30	CTCF	chr13:46197720-46197870	GM12872	blood:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
31	CTCF	chr13:46197740-46197890	Caco-2	colon:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
32	CTCF	chr13:46197080-46197230	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr13:46197609-46198205	IMR90	lung:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
34	CTCF	chr13:46159018-46159208	H1-hESC	embryonic stem cell:	n/a	chr13:46159019-46159027 chr13:46159145-46159163 chr13:46159140-46159161
35	CTCF	chr13:46158980-46159130	HAc	cerebellar:	n/a	chr13:46159019-46159027
36	CTCF	chr13:46198060-46198210	HMF	breast:	n/a	n/a
37	CTCF	chr13:46197676-46197948	HepG2	liver:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
38	CTCF	chr13:46197700-46197850	GM12864	blood:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
39	CTCF	chr13:46197700-46197850	GM12873	blood:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
40	CTCF	chr13:46159040-46159190	HFF-Myc	foreskin:	n/a	chr13:46159145-46159163 chr13:46159140-46159161
41	CTCF	chr13:46197693-46197925	GM10266	blood:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
42	CTCF	chr13:46197680-46197830	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr13:46197760-46197910	HCPEpiC	choroid plexus:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
44	CTCF	chr13:46197690-46197896	NHEK	skin:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
45	CTCF	chr13:46197700-46197850	AG04449	skin:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
46	CTCF	chr13:46159100-46159250	AG04450	lung:	n/a	chr13:46159145-46159163 chr13:46159140-46159161
47	CTCF	chr13:46197740-46197890	GM12865	blood:	n/a	chr13:46197824-46197842 chr13:46197827-46197840 chr13:46197825-46197841 chr13:46197826-46197847
48	CTCF	chr13:46159260-46159410	HCT-116	colon:	n/a	n/a
49	CTCF	chr13:46158980-46159130	NHDF-neo	bronchial:	n/a	chr13:46159019-46159027
50	CTCF	chr13:46159046-46159267	MCF-7	breast:	n/a	chr13:46159145-46159163 chr13:46159140-46159161

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:46190037-46190087	NHDF-neo	bronchial:	n/a
2	chr13:46190037-46190087	NHDF-neo	bronchial:	n/a
3	chr13:46202047-46202097	SK-N-SH_RA	brain:	n/a
4	chr13:46189838-46189888	SK-N-MC	brain:	n/a
5	chr13:46189883-46189933	HRPEpiC	eye:	n/a
6	chr13:46172426-46172476	NH-A	brain:	n/a
7	chr13:46189883-46189933	HIPEpiC	eye:	n/a
8	chr13:46190198-46190248	T-47D	breast:	n/a
9	chr13:46189838-46189888	PFSK-1	brain:	n/a
10	chr13:46159050-46159100	MCF-7	breast:	n/a
11	chr13:46189883-46189933	HRCEpiC	kidney:	n/a
12	chr13:46190028-46190078	IMR90	lung:	fetal
13	chr13:46189838-46189888	HEEpiC	esophagus:	n/a
14	chr13:46190198-46190248	NT2-D1	testis:	n/a
15	chr13:46190098-46190148	AG10803	skin:	n/a
16	chr13:46189883-46189933	NB4	blood:	n/a
17	chr13:46190028-46190078	ProgFib	skin:	n/a
18	chr13:46189906-46189956	CMK	blood:	n/a
19	chr13:46171746-46171796	Hela-S3	cervix:	n/a
20	chr13:46189906-46189956	IMR90	lung:	fetal
21	chr13:46159050-46159100	H1-hESC	embryonic stem cell:	embryo
22	chr13:46189935-46189985	GM12892	blood:	n/a
23	chr13:46159050-46159100	NB4	blood:	n/a
24	chr13:46172426-46172476	HL-60	blood:	n/a
25	chr13:46189906-46189956	HL-60	blood:	n/a
26	chr13:46189935-46189985	U87	brain:	n/a
27	chr13:46202047-46202097	GM12892	blood:	n/a
28	chr13:46189935-46189985	NH-A	brain:	n/a
29	chr13:46190198-46190248	AG10803	skin:	n/a
30	chr13:46189838-46189888	NT2-D1	testis:	n/a
31	chr13:46171746-46171796	HNPCEpiC	eye:	n/a
32	chr13:46189899-46189949	BE2_C	brain:	n/a
33	chr13:46171746-46171796	HRPEpiC	eye:	n/a
34	chr13:46159050-46159100	GM12891	blood:	n/a
35	chr13:46190098-46190148	HepG2	liver:	n/a
36	chr13:46190198-46190248	SKMC	muscle:	n/a
37	chr13:46190028-46190078	K562	blood:	n/a
38	chr13:46202047-46202097	HMEC	breast:	n/a
39	chr13:46202047-46202097	SK-N-MC	brain:	n/a
40	chr13:46190198-46190248	AG09309	skin:	n/a
41	chr13:46190028-46190078	SKMC	muscle:	n/a
42	chr13:46190028-46190078	NH-A	brain:	n/a
43	chr13:46202047-46202097	AoSMC	blood vessel:	n/a
44	chr13:46189838-46189888	Hepatocyte	liver:	n/a
45	chr13:46190028-46190078	PrEC	prostate:	n/a
46	chr13:46189883-46189933	NHDF-neo	bronchial:	n/a
47	chr13:46189838-46189888	HAEpiC	amniotic membrane:	n/a
48	chr13:46190198-46190248	HCF	heart:	n/a
49	chr13:46189906-46189956	A549	lung:	n/a
50	chr13:46190098-46190148	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:46197558..46198457-chr13:46292011..46292949,5	MCF-7	breast:
2	chr13:46206144..46208795-chr13:46225449..46227741,2	MCF-7	breast:
3	chr13:46148680..46151776-chr13:46154310..46157103,3	MCF-7	breast:
4	chr13:46197099..46199094-chr13:46201172..46203433,2	MCF-7	breast:
5	chr13:46166492..46169011-chr13:46171219..46174255,3	MCF-7	breast:
6	chr13:46197542..46198231-chr13:46302675..46303202,2	MCF-7	breast:
7	chr13:46199143..46202004-chr13:46242870..46244667,2	MCF-7	breast:
8	chr13:46159696..46161575-chr20:52534301..52535829,2	MCF-7	breast:
9	chr13:46085576..46086197-chr13:46158674..46159586,2	K562	blood:
10	chr13:46158196..46160607-chr13:46168078..46170279,2	MCF-7	breast:
11	chr13:46158196..46160607-chr13:46168078..46170279,2	MCF-7	breast:
12	chr13:46159453..46160957-chr13:46162948..46164625,2	MCF-7	breast:
13	chr13:46197388..46197903-chr13:46292300..46293039,2	K562	blood:
14	chr13:46197629..46198203-chr13:46291973..46292622,2	MCF-7	breast:
15	chr13:46167136..46169357-chr13:46176565..46178390,2	MCF-7	breast:
16	chr13:46182801..46184932-chr13:46189502..46192160,2	MCF-7	breast:
17	chr13:46197348..46198319-chr13:46895425..46896058,2	K562	blood:
18	chr13:46197381..46198250-chr13:46302335..46303552,6	MCF-7	breast:
19	chr13:46197099..46199094-chr13:46201172..46203433,2	MCF-7	breast:
20	chr13:46197287..46199599-chr13:46586212..46588572,2	MCF-7	breast:
21	chr13:46167136..46169357-chr13:46176565..46178390,2	MCF-7	breast:
22	chr13:46166492..46169011-chr13:46171219..46174255,3	MCF-7	breast:
23	chr13:46197765..46198301-chr13:46584090..46584922,2	MCF-7	breast:
24	chr13:46159453..46160957-chr13:46162948..46164625,2	MCF-7	breast:

Variant related genes	Relation type
FAM194B	TF binding region
FAM194B	CpG island
ENSG00000165837	chromatin interactions

Extended variants
information (count: 1277 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1277 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567869562	chr13:46156804-46156805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs539495615	chr13:46156819-46156820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536900232	chr13:46156876-46156877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7335924	chr13:46156914-46156915	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs570047121	chr13:46156924-46156925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572896954	chr13:46156951-46156952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540808426	chr13:46156955-46156956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs34187119	chr13:46157010-46157011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576321800	chr13:46157013-46157014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs74073914	chr13:46157050-46157051	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs76138082	chr13:46157119-46157120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142874412	chr13:46157149-46157150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74073915	chr13:46157180-46157181	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs187123135	chr13:46157211-46157212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545048736	chr13:46157212-46157213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560205215	chr13:46157284-46157285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527816233	chr13:46157290-46157291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192139580	chr13:46157339-46157340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150657420	chr13:46157362-46157363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs17066941	chr13:46157367-46157368	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs139908293	chr13:46157399-46157400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs74073916	chr13:46157408-46157409	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs568821538	chr13:46157410-46157411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539435145	chr13:46157427-46157428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551434842	chr13:46157478-46157479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183964840	chr13:46157517-46157518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115421098	chr13:46157544-46157545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555897002	chr13:46157593-46157594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531149924	chr13:46158608-46158609	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs17066943	chr13:46158620-46158621	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs114233134	chr13:46158628-46158629	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs76711695	chr13:46158666-46158667	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs554662601	chr13:46158674-46158675	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs549472963	chr13:46158685-46158686	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs571457536	chr13:46158688-46158689	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs376385135	chr13:46158689-46158690	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs74858406	chr13:46158694-46158695	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs187112195	chr13:46158733-46158734	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs2104445	chr13:46158766-46158767	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs536978854	chr13:46158774-46158775	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs554632913	chr13:46158785-46158786	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs576823569	chr13:46158786-46158787	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs191222906	chr13:46158811-46158812	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs182679398	chr13:46158845-46158846	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs3014929	chr13:46158867-46158868	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs386770604	chr13:46158895-46158896	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs80267452	chr13:46158896-46158897	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs553963214	chr13:46158922-46158923	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs576279650	chr13:46158940-46158941	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs146032577	chr13:46158944-46158945	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Ovarian cancer	22355333	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21509527	CNVD
Autism	20841430	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	21088497	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	21750150	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Phyllodes tumor	17334353	CNVD
Retinoblastoma	22278416	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:46156800-46157600	Enhancers	Liver	Liver
2	chr13:46158600-46159000	Bivalent Enhancer	HepG2	liver
3	chr13:46166200-46167200	Enhancers	GM12878-XiMat	blood
4	chr13:46168400-46169400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr13:46168600-46169400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr13:46168800-46169400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:46173400-46173800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr13:46174200-46174400	Enhancers	Psoas Muscle	Psoas
9	chr13:46174400-46175600	Weak transcription	Psoas Muscle	Psoas
10	chr13:46175600-46176400	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr13:46175600-46176800	Enhancers	Psoas Muscle	Psoas
12	chr13:46176000-46176200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr13:46176000-46176800	Enhancers	Fetal Brain Male	brain
14	chr13:46176000-46177000	Enhancers	Fetal Brain Female	brain
15	chr13:46176000-46177000	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr13:46176200-46176800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr13:46176200-46177000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr13:46176200-46177000	Enhancers	Right Atrium	heart
19	chr13:46176400-46176800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr13:46176600-46177800	Enhancers	Fetal Muscle Leg	muscle
21	chr13:46176800-46188600	Weak transcription	Fetal Brain Male	brain
22	chr13:46177000-46184600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr13:46177600-46178000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr13:46178000-46178200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr13:46178200-46179200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr13:46179200-46179400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr13:46179800-46180000	Enhancers	Stomach Mucosa	stomach
28	chr13:46181800-46182600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr13:46182000-46182600	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr13:46185200-46185600	Enhancers	Brain Hippocampus Middle	brain
31	chr13:46185200-46186800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr13:46185400-46185600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr13:46185400-46185600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr13:46185400-46185600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr13:46185400-46185800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr13:46185400-46185800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr13:46185600-46185800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr13:46185600-46185800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr13:46185600-46185800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr13:46185600-46186600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr13:46185600-46189000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr13:46185600-46189000	Weak transcription	Brain Hippocampus Middle	brain
43	chr13:46185800-46189000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr13:46185800-46189200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr13:46186000-46186400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr13:46186400-46186600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr13:46186600-46187200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr13:46187000-46187200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr13:46188400-46188600	Enhancers	H9 Cell Line	embryonic stem cell
50	chr13:46188600-46189000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived

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